Congenital Diaphragmatic HerniaNCT03242044
Resuscitation of Infants With Congenital Diaphragmatic Hernia With an Intact Umbilical Cord
A study testing Congenital diaphragmatic hernia resuscitation with an intact umbilical cord in people with Congenital Diaphragmatic Hernia, run by University of Colorado, Denver at 1 site in United States.
Trial summary
Congenital diaphragmatic hernia (CDH) is a severe birth defect, with a prevalence of 1:2000 to 1:3000 live births where a defect in the diaphragm results in, herniation of the abdominal contents into the chest with subsequent compression of the intrathoracic structures and respiratory insufficiency after birth. Read more about this study
- Who is it for?
- Ages Up to 5 minutes
- Conditions the study is for
- Congenital Diaphragmatic Hernia
- What is being tested?
- Congenital diaphragmatic hernia resuscitation with an intact umbilical cord
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 1 siteUnited States
- Study dates
- 12 Jan 2018to 21 Oct 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 5 minutes
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Pregnant women 18 years of age and older with a fetus with the diagnosis of left and right sided congenital diaphragmatic hernia who consent to the protocol.
Who cannot join
- Patients with Morgagni type defects.
- Infants that have undergone fetal endoscopic tracheal occlusion (FETO)
- Infants with CDH with chromosomal anomalies trisomy 18 and 13
- Infants with bilateral congenital diaphragmatic hernia
Trial locations and contacts
1 site in 1 country.
United States1 site
Children's Hospital Colorado
Aurora, Colorado, 80045
About this study
Congenital diaphragmatic hernia (CDH) is a severe birth defect, with a prevalence of 1:2000 to 1:3000 live births where a defect in the diaphragm results in, herniation of the abdominal contents into the chest with subsequent compression of the intrathoracic structures and respiratory insufficiency after birth. Respiratory insufficiency is managed with intubation and mechanical ventilation. In addition to managing respiratory insufficiency, intubation prevents entrainment of air into the intestines and further compression of the lungs and heart. Resuscitation of infants with CDH also involves placement of a nasogastric tube (NG) into the stomach for removal of entrained air and secretions. As part of routine resuscitation in infants with CDH intubation and NG tube placement are performed after the delivery personnel separates the baby from the placenta by cutting the umbilical cord. This study will assess the feasibility, maternal and fetal tolerance and the optimal approach to performing these initial steps of resuscitation with an intact umbilical cord. The investigators have randomly chosen 10 maternal and infant with congenital diaphragmatic hernia dyads to demonstrate feasibility as well as determine pitfalls and difficulties and the optimal approach to a complex resuscitation with an intact umbilical cord.
Read the detailed description
CDH is a severe birth defect, with a prevalence of 1:2000 to 1:3000 live births where a defect in the diaphragm results in, herniation of the abdominal contents into the chest with subsequent compression of the intrathoracic structures. Compression of the intrathoracic structures results in pulmonary and left ventricular (LV) hypoplasia and abnormal development of the pulmonary vasculature in utero. These abnormalities in the development of the heart and lungs in utero, result in persistent pulmonary hypertension of the newborn (PPHN) and respiratory insufficiency after birth. Respiratory insufficiency is managed with intubation and mechanical ventilation. In addition to managing respiratory insufficiency, intubation prevents entrainment of air into the intestines and further compression of the lungs and heart. As part of routine resuscitation in infants with CDH intubation is performed after the delivery personnel separates the baby from the placenta by cutting the umbilical cord. Resuscitation of infants with CDH also involves placement of a nasogastric tube (NG) into the stomach for removal of entrained air and secretions as well as placement of catheters in the umbilical artery and vein for administration of medications (vein) and continuous blood pressure monitoring and sampling of blood (artery). As part of routine practice at our institution, these initial steps of resuscitation are all performed in parallel such that while one team is intubating and initiating ventilation as well as placing the NG tube, another team is placing umbilical lines. This approach has allowed the investigators to obtain arterial blood gas samples in 20 infants with CDH at a median of 4 minutes of life (range 2-9 minutes). When compared to cord blood arterial samples, pCO2 increases by a median of 35mmHg (range 11-77mmHg) from a median cord ABG pCO2 of 55mmHg (range 28-78 mmHg) to 88mmHg (range 65-123 mmHg). In addition to these changes in pCO2 median base deficit changed from -2 ± 0.5350 in the arterial cord blood sample to -7.994 ± 0.8547 in the umbilical arterial blood sample. The resultant respiratory and metabolic acidosis decreased the pH from 7.289 ± 0.01946 in the arterial cord blood sample to 7.036 ± 0.02051 after birth. In addition to the above measures, as part of routine resuscitation, the investigators routinely obtain echocardiographic studies in the first hour of life, to guide pulmonary hypertension management. These studies demonstrate left ventricular (LV) dysfunction and right to left shunting at the ductus arteriosus about 50% of the time. The investigators speculate that the LV dysfunction and increased pulmonary vascular resistance are at least in part due to the acidemia described above. In addition, decreased preload to the LV from right to left shunting at the ductus arteriosus also likely contributes to LV dysfunction. Standard of care for infants with marked abnormalities in gas exchange and LV dysfunction is ECMO rescue early on in the delivery room.
Clamping of the umbilical cord is one of the first interventions that occurs after birth. This separates the infant from the placenta, signifying a landmark period during which the newborn transforms into an independent entity. The transition from a fetus to a neonate at birth represents a critical phase in our life. Early or immediate cord clamping is standard practice where delivery of the fetus is followed by immediate clamping of the umbilical cord (<15 seconds). In 2010, the International Liaison Committee on Resuscitation (ILCOR) recommended that cord clamping could be delayed for at least 1 min. Since then for low risk infants, delayed cord clamping has become routine with the delivering providers delaying clamping of the cord for 1 minute prior to initiating routine newborn care. In these low risk infants there have been many published reports demonstrating benefit with delayed cord clamping. The benefits are primarily attributed to an increase in neonatal blood volume, secondary to placenta-fetal transfusion. More recently the benefits of delayed cord clamping have been demonstrated in higher risk infants. In preterm infants, delayed cord clamping decreased the need for inotropic support after birth, decreased the need for blood transfusions and reduced the incidence of necrotizing enterocolitis and intraventricular hemorrhage. These improvements appear more in line with improvements in cardiac function, which may or may not be associated with an increase in blood volume. More recently, in infants with congenital heart disease delayed cord clamping has been shown to be feasible and decreased the need for packed red blood cell transfusions after birth. Despite the benefits of delayed cord clamping on both the cardiopulmonary transition as well as postnatal outcomes, delayed cord clamping has never been employed in infants with congenital diaphragmatic hernia. This is due to the need for immediate resuscitation after birth and the risk of adverse outcomes by delaying the initiation of postnatal care.
In a recent study doppler ultrasound was used to measure arterial and venous umbilical blood flow during delayed cord clamping in term vaginal deliveries. After birth, the probe was placed in the middle of the umbilical cord and pattern and duration of flow in vein and arteries were evaluated until cord clamping. In 90% of infants, umbilical venous flow was still present at 4 minutes and 36 seconds. In 83% of infants, umbilical arterial flow was still present at 4 minutes and 22 seconds and in 72% of infants bidirectional arterial flow was observed. Bidirectional arterial flow appeared at 45 seconds after birth and persisted for a median duration of 2 minutes and 24 seconds (01:37- 03:52). This study implies that placental gas exchange may remain active for at least 4-5 minutes after birth and suggests that delaying cord clamping for 4-5 minutes while initiating resuscitation may be feasible.
In fetal sheep, the effect of initiation of ventilation with an intact umbilical cord was studied by placing flow probes around the ductus arteriosus, carotid and pulmonary arteries and catheters in the carotid and pulmonary arteries for direct pressure measurements. With clamping of the umbilical cord prior to initiation of ventilation, carotid artery and pulmonary artery pressure increased, carotid artery blood flow increased initially and then decreased and pulmonary artery blood flow and right ventricular output decreased. These changes in carotid and pulmonary pressure and flow were accompanied by a decrease in heart rate. With just 30 seconds of ventilation prior to clamping of the umbilical cord, the fluctuations in heart rate, carotid and pulmonary artery pressure and flow were prevented and the cardiopulmonary transition was much more stable.
The first published report of resuscitation with an intact umbilical cord compared 24 hour hematocrit in premature infants (23 0/7-31 6/7 weeks' GA) randomized to 60 seconds of V (initial continuous positive airway pressure) with addition of positive pressure ventilation if needed - delayed cord clamping (DCC), V-DCC or DCC-only where infants were dried and stimulated by gently rubbing the back if apneic. In this study no differences were seen in the peak hematocrit in the first 24 hours, delivery room interventions, early hemodynamics (cerebral oxygenation by near-infrared spectroscopy, cardiac output and stroke volume by electrical cardiometry, or superior vena cava flow by functional echocardiography), or neonatal outcomes. The onset of breathing was similar between both groups however infants receiving DCC received a greater duration of stimulation than V-DCC. While no benefit was seen with V-DCC, no adverse effects were seen and this study demonstrated the feasibility of resuscitation with the cord intact. In addition the primary outcome measure differed from our question of interest as the infants enrolled in this study were low risk for abnormalities in the cardiopulmonary transition.
In this protocol, the investigators propose initiation of resuscitation during the period of delayed cord clamping in infants with congenital diaphragmatic hernia. This is a feasibility study that will assess tolerance of the participants (pregnant mother and their high-risk infants) to this method of resuscitation as well as the optimal setup and approach to resuscitation. Tolerance to this approach would provide these infants the benefits of delayed cord clamping while allowing for simultaneous resuscitation. The first aim of this study is to assess maternal and fetal tolerance to the procedure and determine the optimal approach to resuscitation. In addition to this the investigators will assess if initiation of resuscitation during the period of delayed cord clamping can stabilize gas exchange and prevent the hypercarbia and acidosis that ensues after birth. Due to the physiologic effects of initiation of ventilation prior to clamping of the umbilical cord the investigators hypothesize that initiation of resuscitation prior to umbilical cord clamping will stabilize the cardiopulmonary transition and will decrease the prevalence of LV dysfunction in this population. The results of this study will lay the foundation for a future multi-center randomized trial and are likely to impact the manner in which newborns with CDH are resuscitated after birth
- Conditions
- Congenital Diaphragmatic Hernia
- Being tested
- Congenital diaphragmatic hernia resuscitation with an intact umbilical cord
- Medical subject headings
- Hernias, Diaphragmatic, Congenital
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Congenital diaphragmatic hernia resuscitation with an intact umbilical cordProcedure or surgery
10 infants with left or right sided congenital diaphragmatic hernia will be intubated and ventilation initiated while still attached to the placental circulation through the umbilical cord. In addition, at the same time, a nasogastric tube will be placed in the stomach to drain entrained air and secretions. After 5 minutes of resuscitation with the umbilical cord intact, the umbilical cord will be cut, infants separated from the placenta and resuscitation performed per routine neonatal resuscitation protocols. Feasibility, the optimal approach and maternal and infant tolerance to the procedure will be assessed as part of the study.
| Study group | Role | What they receive |
|---|---|---|
| Resuscitation with intact umbilical cord | Experimental | This is a one arm study. Pregnant women greater than 18 years of age with a fetus with left or right sided congenital diaphragmatic hernia of age that consent to the protocol will be enrolled in the study. This is a pilot feasibility study that will assess maternal and infant tolerance to resuscitation with an intact umbilical cord as well as the optimal method for performing an advanced resuscitation with the umbilical cord intact. For this reason patients will not be randomized. Receives: Procedure: Congenital diaphragmatic hernia resuscitation with an intact umbilical cord |
What is being measured
The primary outcome is the main question the study is designed to answer.
Tolerance of resuscitation on infants with congenital diaphragmatic hernia with an intact umbilical cord.
10 maternal and infant with left or right sided congenital diaphragmatic hernia dyads will be enrolled in the study and maternal and infant tolerance to resuscitation with an intact umbilical cord determined. Maternal tolerance will be assessed by the incidence of post-partum hemorrhage and uterine atony, infant tolerance determined by capillary blood gas assessments of pH, pCO2 and base deficit and the incidence of bradycardia lasting greater than 1 minute.
Measured: 5 minutes
Secondary outcomes (3)
Feasibility of resuscitation on infants with congenital diaphragmatic hernia with an intact umbilical cord.
10 maternal and infant with left or right sided congenital diaphragmatic hernia dyads will be enrolled in the study and feasibility of performing a complex resuscitation with an intact umbilical cord assessed. Feasibility will be assessed by feedback from resuscitation participants as well as efficiency of the resuscitation when compared to historical controls. As part of feasibility the optimal approach to performing the resuscitation with the umbilical cord intact will be determined.
Measured: 5 minutes
Evaluation of Infant gas exchange after clamping the umbilical cord
10 maternal and infant with left or right sided congenital diaphragmatic hernia dyads will be enrolled in the study and after 5 minutes of resuscitation with an intact umbilical cord, the cord will be cut and the infant separated from the mother. Umbilical venous and arterial catheters will be placed and arterial blood gas drawn to assess arterial pH, pCO2, PaO2 and base deficit.
Measured: 10 minutes
Left ventricular function after resuscitation with an intact umbilical cord
10 maternal and infant with left or right sided congenital diaphragmatic hernia dyads will be enrolled in the study and after 5 minutes of resuscitation with an intact umbilical cord, the cord will be cut and the infant separated from the mother. Following separation from the mother echocardiography will be performed on the infant and left ventricular function measured.
Measured: 20 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Aug 2017
- Study start12 Jan 2018
- Primary completion21 Oct 2020
- Study completion21 Oct 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (21)Papers the sponsor has linked to this study.
- Other trials for Congenital Diaphragmatic HerniaStudies of the same condition, open and under way.
- More trials run by University of Colorado, DenverThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- This is a pilot feasibility study that will assess maternal and infant tolerance to the protocols as well as the optimal method for performing an advanced resuscitation with an intact umbilical cord. The investigators have randomly chosen 10 study participant to make this assessment and determine methodologies. For this reason study participants will not be randomized. Pregnant women greater than 18 years of age that consent to the protocol will be enrolled in the study arm.
- Masking
- None (open label)
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Colorado, Denver
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Jason Gien, MD, Principal investigator, University of Colorado, Denver
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03242044
- Sponsor's protocol ID
- 17-0788
- Status last verified
- Jun 2021
- First submitted
- 26 Jul 2017
- Last updated
- 14 Jun 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Results of the study when completed will be published in a peer review journal
Publications
Torfs CP, Curry CJ, Bateson TF, Honore LH. A population-based study of congenital diaphragmatic hernia. Teratology. 1992 Dec;46(6):555-65. doi: 10.1002/tera.1420460605.
PubMed 1290156Skari H, Bjornland K, Haugen G, Egeland T, Emblem R. Congenital diaphragmatic hernia: a meta-analysis of mortality factors. J Pediatr Surg. 2000 Aug;35(8):1187-97. doi: 10.1053/jpsu.2000.8725.
PubMed 10945692Harrison MR, Adzick NS, Nakayama DK, deLorimier AA. Fetal diaphragmatic hernia: pathophysiology, natural history, and outcome. Clin Obstet Gynecol. 1986 Sep;29(3):490-501. No abstract available.
PubMed 3757331Schwartz SM, Vermilion RP, Hirschl RB. Evaluation of left ventricular mass in children with left-sided congenital diaphragmatic hernia. J Pediatr. 1994 Sep;125(3):447-51. doi: 10.1016/s0022-3476(05)83293-7.
PubMed 8071756Vogel M, McElhinney DB, Marcus E, Morash D, Jennings RW, Tworetzky W. Significance and outcome of left heart hypoplasia in fetal congenital diaphragmatic hernia. Ultrasound Obstet Gynecol. 2010 Mar;35(3):310-7. doi: 10.1002/uog.7497.
PubMed 20143332Taira Y, Yamataka T, Miyazaki E, Puri P. Comparison of the pulmonary vasculature in newborns and stillborns with congenital diaphragmatic hernia. Pediatr Surg Int. 1998 Nov;14(1-2):30-5. doi: 10.1007/s003830050429.
PubMed 9880691Van Loenhout RB, De Krijger RR, Van de Ven CP, Van der Horst IW, Beurskens LW, Tibboel D, Keijzer R. Postmortem biopsy to obtain lung tissue in congenital diaphragmatic hernia. Neonatology. 2013;103(3):213-7. doi: 10.1159/000345921. Epub 2013 Jan 12.
PubMed 23328121Reiss I, Schaible T, van den Hout L, Capolupo I, Allegaert K, van Heijst A, Gorett Silva M, Greenough A, Tibboel D; CDH EURO Consortium. Standardized postnatal management of infants with congenital diaphragmatic hernia in Europe: the CDH EURO Consortium consensus. Neonatology. 2010;98(4):354-64. doi: 10.1159/000320622. Epub 2010 Oct 27.
PubMed 20980772Biban P, Filipovic-Grcic B, Biarent D, Manzoni P; International Liaison Committee on Resuscitation (ILCOR); European Resuscitation Council (ERC); American Heart Association (AHA); American Academy of Pediatrics (AAP). New cardiopulmonary resuscitation guidelines 2010: managing the newly born in delivery room. Early Hum Dev. 2011 Mar;87 Suppl 1:S9-11. doi: 10.1016/j.earlhumdev.2011.01.002. Epub 2011 Jan 19.
PubMed 21251771Niermeyer S, Velaphi S. Promoting physiologic transition at birth: re-examining resuscitation and the timing of cord clamping. Semin Fetal Neonatal Med. 2013 Dec;18(6):385-92. doi: 10.1016/j.siny.2013.08.008. Epub 2013 Sep 19.
PubMed 24055300Rabe H, Diaz-Rossello JL, Duley L, Dowswell T. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2012 Aug 15;(8):CD003248. doi: 10.1002/14651858.CD003248.pub3.
PubMed 22895933Committee Opinion No. 684: Delayed Umbilical Cord Clamping After Birth. Obstet Gynecol. 2017 Jan;129(1):1. doi: 10.1097/AOG.0000000000001860.
PubMed 28002310Baenziger O, Stolkin F, Keel M, von Siebenthal K, Fauchere JC, Das Kundu S, Dietz V, Bucher HU, Wolf M. The influence of the timing of cord clamping on postnatal cerebral oxygenation in preterm neonates: a randomized, controlled trial. Pediatrics. 2007 Mar;119(3):455-9. doi: 10.1542/peds.2006-2725.
PubMed 17332197Vesoulis ZA, Rhoades J, Muniyandi P, Conner S, Cahill AG, Mathur AM. Delayed cord clamping and inotrope use in preterm infants. J Matern Fetal Neonatal Med. 2018 May;31(10):1327-1334. doi: 10.1080/14767058.2017.1315663. Epub 2017 Apr 20.
PubMed 28372510Rabe H, Reynolds G, Diaz-Rossello J. A systematic review and meta-analysis of a brief delay in clamping the umbilical cord of preterm infants. Neonatology. 2008;93(2):138-44. doi: 10.1159/000108764. Epub 2007 Sep 21.
PubMed 17890882
Study at a glance
From the registry record, last updated by the sponsor on 14 Jun 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Resuscitation of Infants With Congenital Diaphragmatic Hernia With an Intact Umbilical Cord
- ClinicalTrials.gov ID
- NCT03242044
- Acronym / sponsor ID
- 17-0788
- Conditions
- Congenital Diaphragmatic Hernia
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 10 participants (actual)
- Lead sponsor
- University of Colorado, DenverUniversity, hospital or other
- Study start
- 12 Jan 2018 (actual)
- Primary completion
- 21 Oct 2020 (actual)
- Study completion
- 21 Oct 2020 (actual)
- First posted
- 8 Aug 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Congenital diaphragmatic hernia (CDH) is a severe birth defect, with a prevalence of 1:2000 to 1:3000 live births where a defect in the diaphragm results in, herniation of the abdominal contents into the chest with subsequent compression of the intrathoracic structures and respiratory insufficiency after birth. Respiratory insufficiency is managed with intubation and mechanical ventilation. In addition to managing respiratory insufficiency, intubation prevents entrainment of air into the intestines and further compression of the lungs and heart. Resuscitation of infants with CDH also involves placement of a nasogastric tube (NG) into the stomach for removal of entrained air and secretions. As part of routine resuscitation in infants with CDH intubation and NG tube placement are performed after the delivery personnel separates the baby from the placenta by cutting the umbilical cord. This study will assess the feasibility, maternal and fetal tolerance and the optimal approach to performing these initial steps of resuscitation with an intact umbilical cord. The investigators have randomly chosen 10 maternal and infant with congenital diaphragmatic hernia dyads to demonstrate feasibility as well as determine pitfalls and difficulties and the optimal approach to a complex resuscitation with an intact umbilical cord.
Detailed description
CDH is a severe birth defect, with a prevalence of 1:2000 to 1:3000 live births where a defect in the diaphragm results in, herniation of the abdominal contents into the chest with subsequent compression of the intrathoracic structures. Compression of the intrathoracic structures results in pulmonary and left ventricular (LV) hypoplasia and abnormal development of the pulmonary vasculature in utero. These abnormalities in the development of the heart and lungs in utero, result in persistent pulmonary hypertension of the newborn (PPHN) and respiratory insufficiency after birth. Respiratory insufficiency is managed with intubation and mechanical ventilation. In addition to managing respiratory insufficiency, intubation prevents entrainment of air into the intestines and further compression of the lungs and heart. As part of routine resuscitation in infants with CDH intubation is performed after the delivery personnel separates the baby from the placenta by cutting the umbilical cord. Resuscitation of infants with CDH also involves placement of a nasogastric tube (NG) into the stomach for removal of entrained air and secretions as well as placement of catheters in the umbilical artery and vein for administration of medications (vein) and continuous blood pressure monitoring and sampling of blood (artery). As part of routine practice at our institution, these initial steps of resuscitation are all performed in parallel such that while one team is intubating and initiating ventilation as well as placing the NG tube, another team is placing umbilical lines. This approach has allowed the investigators to obtain arterial blood gas samples in 20 infants with CDH at a median of 4 minutes of life (range 2-9 minutes). When compared to cord blood arterial samples, pCO2 increases by a median of 35mmHg (range 11-77mmHg) from a median cord ABG pCO2 of 55mmHg (range 28-78 mmHg) to 88mmHg (range 65-123 mmHg). In addition to these changes in pCO2 median base deficit changed from -2 ± 0.5350 in the arterial cord blood sample to -7.994 ± 0.8547 in the umbilical arterial blood sample. The resultant respiratory and metabolic acidosis decreased the pH from 7.289 ± 0.01946 in the arterial cord blood sample to 7.036 ± 0.02051 after birth. In addition to the above measures, as part of routine resuscitation, the investigators routinely obtain echocardiographic studies in the first hour of life, to guide pulmonary hypertension management. These studies demonstrate left ventricular (LV) dysfunction and right to left shunting at the ductus arteriosus about 50% of the time. The investigators speculate that the LV dysfunction and increased pulmonary vascular resistance are at least in part due to the acidemia described above. In addition, decreased preload to the LV from right to left shunting at the ductus arteriosus also likely contributes to LV dysfunction. Standard of care for infants with marked abnormalities in gas exchange and LV dysfunction is ECMO rescue early on in the delivery room.
Clamping of the umbilical cord is one of the first interventions that occurs after birth. This separates the infant from the placenta, signifying a landmark period during which the newborn transforms into an independent entity. The transition from a fetus to a neonate at birth represents a critical phase in our life. Early or immediate cord clamping is standard practice where delivery of the fetus is followed by immediate clamping of the umbilical cord (<15 seconds). In 2010, the International Liaison Committee on Resuscitation (ILCOR) recommended that cord clamping could be delayed for at least 1 min. Since then for low risk infants, delayed cord clamping has become routine with the delivering providers delaying clamping of the cord for 1 minute prior to initiating routine newborn care. In these low risk infants there have been many published reports demonstrating benefit with delayed cord clamping. The benefits are primarily attributed to an increase in neonatal blood volume, secondary to placenta-fetal transfusion. More recently the benefits of delayed cord clamping have been demonstrated in higher risk infants. In preterm infants, delayed cord clamping decreased the need for inotropic support after birth, decreased the need for blood transfusions and reduced the incidence of necrotizing enterocolitis and intraventricular hemorrhage. These improvements appear more in line with improvements in cardiac function, which may or may not be associated with an increase in blood volume. More recently, in infants with congenital heart disease delayed cord clamping has been shown to be feasible and decreased the need for packed red blood cell transfusions after birth. Despite the benefits of delayed cord clamping on both the cardiopulmonary transition as well as postnatal outcomes, delayed cord clamping has never been employed in infants with congenital diaphragmatic hernia. This is due to the need for immediate resuscitation after birth and the risk of adverse outcomes by delaying the initiation of postnatal care.
In a recent study doppler ultrasound was used to measure arterial and venous umbilical blood flow during delayed cord clamping in term vaginal deliveries. After birth, the probe was placed in the middle of the umbilical cord and pattern and duration of flow in vein and arteries were evaluated until cord clamping. In 90% of infants, umbilical venous flow was still present at 4 minutes and 36 seconds. In 83% of infants, umbilical arterial flow was still present at 4 minutes and 22 seconds and in 72% of infants bidirectional arterial flow was observed. Bidirectional arterial flow appeared at 45 seconds after birth and persisted for a median duration of 2 minutes and 24 seconds (01:37- 03:52). This study implies that placental gas exchange may remain active for at least 4-5 minutes after birth and suggests that delaying cord clamping for 4-5 minutes while initiating resuscitation may be feasible.
In fetal sheep, the effect of initiation of ventilation with an intact umbilical cord was studied by placing flow probes around the ductus arteriosus, carotid and pulmonary arteries and catheters in the carotid and pulmonary arteries for direct pressure measurements. With clamping of the umbilical cord prior to initiation of ventilation, carotid artery and pulmonary artery pressure increased, carotid artery blood flow increased initially and then decreased and pulmonary artery blood flow and right ventricular output decreased. These changes in carotid and pulmonary pressure and flow were accompanied by a decrease in heart rate. With just 30 seconds of ventilation prior to clamping of the umbilical cord, the fluctuations in heart rate, carotid and pulmonary artery pressure and flow were prevented and the cardiopulmonary transition was much more stable.
The first published report of resuscitation with an intact umbilical cord compared 24 hour hematocrit in premature infants (23 0/7-31 6/7 weeks' GA) randomized to 60 seconds of V (initial continuous positive airway pressure) with addition of positive pressure ventilation if needed - delayed cord clamping (DCC), V-DCC or DCC-only where infants were dried and stimulated by gently rubbing the back if apneic. In this study no differences were seen in the peak hematocrit in the first 24 hours, delivery room interventions, early hemodynamics (cerebral oxygenation by near-infrared spectroscopy, cardiac output and stroke volume by electrical cardiometry, or superior vena cava flow by functional echocardiography), or neonatal outcomes. The onset of breathing was similar between both groups however infants receiving DCC received a greater duration of stimulation than V-DCC. While no benefit was seen with V-DCC, no adverse effects were seen and this study demonstrated the feasibility of resuscitation with the cord intact. In addition the primary outcome measure differed from our question of interest as the infants enrolled in this study were low risk for abnormalities in the cardiopulmonary transition.
In this protocol, the investigators propose initiation of resuscitation during the period of delayed cord clamping in infants with congenital diaphragmatic hernia. This is a feasibility study that will assess tolerance of the participants (pregnant mother and their high-risk infants) to this method of resuscitation as well as the optimal setup and approach to resuscitation. Tolerance to this approach would provide these infants the benefits of delayed cord clamping while allowing for simultaneous resuscitation. The first aim of this study is to assess maternal and fetal tolerance to the procedure and determine the optimal approach to resuscitation. In addition to this the investigators will assess if initiation of resuscitation during the period of delayed cord clamping can stabilize gas exchange and prevent the hypercarbia and acidosis that ensues after birth. Due to the physiologic effects of initiation of ventilation prior to clamping of the umbilical cord the investigators hypothesize that initiation of resuscitation prior to umbilical cord clamping will stabilize the cardiopulmonary transition and will decrease the prevalence of LV dysfunction in this population. The results of this study will lay the foundation for a future multi-center randomized trial and are likely to impact the manner in which newborns with CDH are resuscitated after birth
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- This is a pilot feasibility study that will assess maternal and infant tolerance to the protocols as well as the optimal method for performing an advanced resuscitation with an intact umbilical cord. The investigators have randomly chosen 10 study participant to make this assessment and determine methodologies. For this reason study participants will not be randomized. Pregnant women greater than 18 years of age that consent to the protocol will be enrolled in the study arm.
| Arm | Type | Receives |
|---|---|---|
| Resuscitation with intact umbilical cord | Experimental | Procedure: Congenital diaphragmatic hernia resuscitation with an intact umbilical cordThis is a one arm study. Pregnant women greater than 18 years of age with a fetus with left or right sided congenital diaphragmatic hernia of age that consent to the protocol will be enrolled in the study. This is a pilot feasibility study that will assess maternal and infant tolerance to resuscitation with an intact umbilical cord as well as the optimal method for performing an advanced resuscitation with the umbilical cord intact. For this reason patients will not be randomized. |
Who may qualify
- Ages
- Up to 5 minutes
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Pregnant women 18 years of age and older with a fetus with the diagnosis of left and right sided congenital diaphragmatic hernia who consent to the protocol.
Key exclusion criteria (4 listed)
- Patients with Morgagni type defects.
- Infants that have undergone fetal endoscopic tracheal occlusion (FETO)
- Infants with CDH with chromosomal anomalies trisomy 18 and 13
- Infants with bilateral congenital diaphragmatic hernia
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Congenital diaphragmatic hernia resuscitation with an intact umbilical cord10 infants with left or right sided congenital diaphragmatic hernia will be intubated and ventilation initiated while still attached to the placental circulation through the umbilical cord. In addition, at the same time, a nasogastric tube will be placed in the stomach to drain entrained air and secretions. After 5 minutes of resuscitation with the umbilical cord intact, the umbilical cord will be cut, infants separated from the placenta and resuscitation performed per routine neonatal resuscitation protocols. Feasibility, the optimal approach and maternal and infant tolerance to the procedure will be assessed as part of the study. | Procedure or surgery | Resuscitation with intact umbilical cord |
Primary outcome
Tolerance of resuscitation on infants with congenital diaphragmatic hernia with an intact umbilical cord.
Time frame: 5 minutes
10 maternal and infant with left or right sided congenital diaphragmatic hernia dyads will be enrolled in the study and maternal and infant tolerance to resuscitation with an intact umbilical cord determined. Maternal tolerance will be assessed by the incidence of post-partum hemorrhage and uterine atony, infant tolerance determined by capillary blood gas assessments of pH, pCO2 and base deficit and the incidence of bradycardia lasting greater than 1 minute.
3 secondary outcomes
Feasibility of resuscitation on infants with congenital diaphragmatic hernia with an intact umbilical cord.
Time frame: 5 minutes
Evaluation of Infant gas exchange after clamping the umbilical cord
Time frame: 10 minutes
Left ventricular function after resuscitation with an intact umbilical cord
Time frame: 20 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jun 2021.
- Results publication: PubMed 1290156Torfs CP, Curry CJ, Bateson TF, Honore LH. A population-based study of congenital diaphragmatic hernia. Teratology. 1992 Dec;46(6):555-65. doi: 10.1002/tera.1420460605.
- Results publication: PubMed 10945692Skari H, Bjornland K, Haugen G, Egeland T, Emblem R. Congenital diaphragmatic hernia: a meta-analysis of mortality factors. J Pediatr Surg. 2000 Aug;35(8):1187-97. doi: 10.1053/jpsu.2000.8725.
- Results publication: PubMed 3757331Harrison MR, Adzick NS, Nakayama DK, deLorimier AA. Fetal diaphragmatic hernia: pathophysiology, natural history, and outcome. Clin Obstet Gynecol. 1986 Sep;29(3):490-501. No abstract available.
- Results publication: PubMed 8071756Schwartz SM, Vermilion RP, Hirschl RB. Evaluation of left ventricular mass in children with left-sided congenital diaphragmatic hernia. J Pediatr. 1994 Sep;125(3):447-51. doi: 10.1016/s0022-3476(05)83293-7.
- Results publication: PubMed 20143332Vogel M, McElhinney DB, Marcus E, Morash D, Jennings RW, Tworetzky W. Significance and outcome of left heart hypoplasia in fetal congenital diaphragmatic hernia. Ultrasound Obstet Gynecol. 2010 Mar;35(3):310-7. doi: 10.1002/uog.7497.
- Results publication: PubMed 9880691Taira Y, Yamataka T, Miyazaki E, Puri P. Comparison of the pulmonary vasculature in newborns and stillborns with congenital diaphragmatic hernia. Pediatr Surg Int. 1998 Nov;14(1-2):30-5. doi: 10.1007/s003830050429.
- Results publication: PubMed 23328121Van Loenhout RB, De Krijger RR, Van de Ven CP, Van der Horst IW, Beurskens LW, Tibboel D, Keijzer R. Postmortem biopsy to obtain lung tissue in congenital diaphragmatic hernia. Neonatology. 2013;103(3):213-7. doi: 10.1159/000345921. Epub 2013 Jan 12.
- Results publication: PubMed 20980772Reiss I, Schaible T, van den Hout L, Capolupo I, Allegaert K, van Heijst A, Gorett Silva M, Greenough A, Tibboel D; CDH EURO Consortium. Standardized postnatal management of infants with congenital diaphragmatic hernia in Europe: the CDH EURO Consortium consensus. Neonatology. 2010;98(4):354-64. doi: 10.1159/000320622. Epub 2010 Oct 27.
- Results publication: PubMed 21251771Biban P, Filipovic-Grcic B, Biarent D, Manzoni P; International Liaison Committee on Resuscitation (ILCOR); European Resuscitation Council (ERC); American Heart Association (AHA); American Academy of Pediatrics (AAP). New cardiopulmonary resuscitation guidelines 2010: managing the newly born in delivery room. Early Hum Dev. 2011 Mar;87 Suppl 1:S9-11. doi: 10.1016/j.earlhumdev.2011.01.002. Epub 2011 Jan 19.
- Results publication: PubMed 24055300Niermeyer S, Velaphi S. Promoting physiologic transition at birth: re-examining resuscitation and the timing of cord clamping. Semin Fetal Neonatal Med. 2013 Dec;18(6):385-92. doi: 10.1016/j.siny.2013.08.008. Epub 2013 Sep 19.
- Results publication: PubMed 22895933Rabe H, Diaz-Rossello JL, Duley L, Dowswell T. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2012 Aug 15;(8):CD003248. doi: 10.1002/14651858.CD003248.pub3.
- Results publication: PubMed 28002310Committee Opinion No. 684: Delayed Umbilical Cord Clamping After Birth. Obstet Gynecol. 2017 Jan;129(1):1. doi: 10.1097/AOG.0000000000001860.
- Individual participant dataSharing planned: No. Results of the study when completed will be published in a peer review journal
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jason Gien, MD principal investigator
University of Colorado, Denver
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Congenital diaphragmatic hernia resuscitation with an intact umbilical cord in people with Congenital Diaphragmatic Hernia, run by University of Colorado, Denver at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Jun 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Tolerance of resuscitation on infants with congenital diaphragmatic hernia with an intact umbilical cord. (time frame: 5 minutes). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03242044, which also lists 21 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2021.