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Transient Tachypnea of the NewbornNCT06270823

Reducing Respiratory Distress After Elective Caesarean Birth Through Knee-chest-flexion: a Randomized Controlled Trial

A study testing Knee-to-chest-flexion manoeuvre in people with Transient Tachypnea of the Newborn, run by Kilimanjaro Clinical Research Institute at 1 site in Tanzania.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Planned caesarean birth is a risk factor for the development of neonatal respiratory distress commonly known as transient tachypnoea of the newborn. This is due to the absence of labor physiology which facilitates the clearance of fetal lung fluid. Read more about this study

Who is it for?
Ages Up to 30 minutes
Conditions the study is for
Transient Tachypnea of the Newborn
What is being tested?
Knee-to-chest-flexion manoeuvre
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
562 participants
Where
1 siteTanzania
Study dates
14 Feb 2024to 14 Feb 2025
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 30 minutes
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Infants born by planned CS, 37-42 weeks gestational age

Who cannot join

  • infants with significant congenital malformations influencing cardiopulmonary transition
  • infants whose mother has gestational diabetes, pre-eclampsia, eclampsia
  • infants where immediate cord clamping is needed due to resuscitation of the baby or mother
  • when spontaneous contractions before the cesarean section is done.
  • KCF will not be done to infants who will start breathing instantly after being extracted from the uterus so as not to interfere with their breathing efforts

Trial locations and contacts

1 site in 1 country.

Febronia L Shirima, MD contact

+255714143368

febbylaw17@gmail.com

Tupokigwe Jana contact

+255784734602

t.jana@kcri.ac.tz

Tanzania1 site, 1 recruiting
  • Kilimanjaro Christian Medical Centre

    Moshi, Kilimanjaro, P.O.Box 3010

    Febronia L Shirima, MD, +255714143368, febbylaw17@gmail.com

    Bariki Mchome, PhD, +255784280027, barikimchome@gmail.com

    Recruiting

Other trials in Tanzania

About this study

Official title: Making Elective Caesarean Safer for Infant's Lungs by Reducing Respiratory Distress Using Knee-chest-flexion: a Randomized Controlled Trial

Planned caesarean birth is a risk factor for the development of neonatal respiratory distress commonly known as transient tachypnoea of the newborn. This is due to the absence of labor physiology which facilitates the clearance of fetal lung fluid. We hypothesized that by mimicking flexion induced by uterine contractions by manually performing knee-to-chest flexion directly at birth to achieve expulsion of excess lung liquid, we could reduce the incidence of respiratory distress in term children born by planned CS.

The goal of this clinical trial is to test whether performing a knee-to-chest flexion maneuver directly after elective caesarean section will decrease the incidence of respiratory distress in term infants when compared to the standard care

Read the detailed description

One of the major risk factors for term/near-term infants to develop respiratory distress (RD) is when they are born by elective caesarean section (CS). While this form of RD, commonly diagnosed as transient tachypnea of the newborn (TTN), is considered to be self-limiting, the severity of RD often leads to unexpected admission to the pediatric ward for respiratory support. TTN has also been associated and asthma, bronchiolitis, and other wheezing syndromes later in life. In low- and middle-income settings, where neonatal intensive care resources are limited, a considerable proportion of babies in need of respiratory support do not survive.

There is now strong physiological evidence that RD after elective cesarean section is caused by this greater volume of airway liquid present at birth, which is due to the absence of labor. During labor, uterine contractions contribute to the flexion of the fetus which increases abdominal and transpulmonary pressure. This elevates the diaphragm, resulting in lung liquid loss via nose and mouth. Flexion induced by uterine contractions could be mimicked by manually performing knee-to-chest flexion directly at birth, to achieve expulsion of excess lung liquid. When applying KCF, we essentially bring the newborn back into fetal position, similar to the holding position applied for performing lumbar puncture in neonates.

If this simple intervention has shown to improve neonatal outcome in the clinical setting, KCF will undoubtedly be an extremely cost-effective health care innovation. The maneuver is easy-to-teach to any clinician performing cesarean section. KCF will be performed conform standard gentle care and is likely to be entirely harmless. These advantages (easy-to-teach, no cost, no harm) are relevant across all settings, but may be particularly appealing in low-income settings, where neonatal follow-up and access to neonatal intensive care are often either impossible or limited. It is therefore of outmost importance to test this intervention in a larger institution adapted to performing high-quality clinical research in a low- or middle-income country.

We now hypothesize that performing a knee-to-chest flexion performed directly after birth will reduce the incidence of respiratory distress in term children born by elective caesarean section.

Objective: To test whether performing a knee-to-chest flexion (KCF) manoeuvre directly after elective CS will decrease the incidence of respiratory distress in term infants when compared to standard care.

Study design: Single-center randomized controlled trial Study population: Infants born by elective CS, 37-42 weeks gestational age. Simple randomization will be done to assign participants in either an interventional group or a control group Intervention: As soon as the infant is out of the uterus a KCF is performed for 30 seconds while the infant remains attached to the cord. Except for KCF, the infant will receive normal routine care and there are no co-interventions.

Control: As soon as the infant is out of the uterus normal routine care is given.

Study parameters: The primary outcome is the occurrence of respiratory distress

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

In the group of term infants born after elective caesarean there is a 7% risk for respiratory distress, of which 10% is complicated by PPHN. Although KCF is a new intervention performed directly after birth for 30 seconds, the technique used is similar to the way infants are held and positioned during a lumbar puncture. As the infants in this study population are in good condition before birth and would otherwise also have been exposed to large intrathoracic pressures generated by uterine contractions during labor, we expect that there is no added risk when the maneuver is performed gently and with care. We recently demonstrated that performing KCF directly after birth is feasible and safe after elective CS. As the percentages of elective CS are increasing worldwide both in developing and developed countries, there is a large potential to reduce morbidity, admissions at NICU and pediatric wards, and healthcare costs in this group of infants.

Being tested
Knee-to-chest-flexion manoeuvre
Keywords
planned caesarean birth
Medical subject headings
Transient Tachypnea of the Newborn

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Knee-to-chest-flexion manoeuvreProcedure or surgery

    The obstetrician will place one hand at the neck and shoulder of the baby and gently bend the infant into dorsiflexion while with the other hand bending the hips and knees against the abdomen and chest (squatting into fetal position). This holding position will be continued for 30 seconds, while compression of the umbilical cord is avoided to maintain an undisturbed umbilical circulation to and from the infant during KCF.

Study groups in NCT06270823
Study groupRoleWhat they receive
interventional armExperimentalAs soon as the infant is out of the uterus a Knee-to-chest flexion (KCF) maneuver is performed for 30 seconds while the infant remains attached to the cord. When applying KCF, we essentially bring the newborn back into the fetal position, flexing the knees to the chest. This is similar to the holding position applied for performing lumbar puncture in neonates. Except for KCF, the infant will receive normal routine care and there are no co-interventions.
Receives: Procedure: Knee-to-chest-flexion manoeuvre
controlNo interventionAs soon as the infant is out of the uterus normal routine care is given

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. respiratory distress

    newborns who have any signs of respiratory distress such as tachypnoea, nasal flaring, chest indrawing, grunting, cyanosis

    Measured: 24 hours

Secondary outcomes (1)
  1. adverse outcome of knee-to-chest flexion maneuver

    any signs of adverse outcomes from knee to chest flexion maneuver such as Hematoma on extremities, abdomen, or chest within 24 hours after birth

    Measured: 24hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Feb 2024
  2. Study start14 Feb 2024
  3. Primary completion14 Feb 2025 (estimated)
  4. Study completion14 Feb 2025 (estimated)

Resources

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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
562 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06270823
Sponsor's protocol ID
NIMR/HQ/R.8a/Vol.IX/4331
Status last verified
Feb 2024
First submitted
14 Feb 2024
Last updated
21 Feb 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Individual Participant Data that underlies results in a publication will be shared

Publications

  • Shirima FL, Manteiga KR, Mchome B, Keus A, Mmbaga BT, Te Pas AB, van den Akker T. Acceptability of the knee-to-chest flexion maneuver to reduce neonatal respiratory distress after elective cesarean section: a qualitative study among healthcare providers. J Matern Fetal Neonatal Med. 2026 Dec;39(1):2666475. doi: 10.1080/14767058.2026.2666475. Epub 2026 May 6.

    PubMed 42091518
  • Shirima FL, Keus A, Mchome B, Mangi G, Davies I, van den Akker T, Mmbaga BT, Hooper SB, Te Pas AB. The effectiveness of knee-chest-flexion maneuver in reducing respiratory distress in elective cesarean section newborns: protocol for a randomized controlled trial. Contemp Clin Trials. 2025 Sep;156:108006. doi: 10.1016/j.cct.2025.108006. Epub 2025 Jul 11.

    PubMed 40653309

Questions about this trial

What is this clinical trial studying?

A study testing Knee-to-chest-flexion manoeuvre in people with Transient Tachypnea of the Newborn, run by Kilimanjaro Clinical Research Institute at 1 site in Tanzania.

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 5 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: status not confirmed, as of the sponsor's last update on 21 Feb 2024. 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 Tanzania. 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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Febronia L Shirima, MD (+255714143368, febbylaw17@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

respiratory distress (time frame: 24 hours). 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 NCT06270823, which also lists 2 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 21 Feb 2024.

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