Esophageal AtresiaPhase 2NCT03127345
Omega 3 Fatty Acid Treatment for Pediatric Musculoskeletal Health
A Phase 2 study testing Omegaven and Intralipid in people with Esophageal Atresia, run by Boston Children's Hospital.
Trial summary
This is a randomized clinical trial comparing Omegaven® treatment with standard of care (soybean-based lipid formulation, Intralipid®) on bone health outcomes in infants with esophageal atresia (EA) undergoing surgical repair at Boston Children's Hospital. Read more about this study
- Who is it for?
- Ages Up to 12 months
- Conditions the study is for
- Esophageal Atresia
- What is being tested?
- Omegaven and Intralipid
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- No sites listed yet
- Study dates
- Sep 2019to Sep 2023
- Phase
- Phase 2
- 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 12 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- 1) Diagnosis of long-gap EA (esophageal gap length >3cm) 2) Age <12 months (not yet reached 12 month birthday) 3) Anticipated surgical repair for management of EA utilizing esophageal traction requiring prolonged intubation, muscle relaxation, and parenteral nutrition dependence.
- Known genetic bone disease, including osteogenesis imperfecta, idiopathic infantile hypercalcemia, and vitamin D resistant rickets
- Prior fragility fracture (including humerus or femur)
- Anticipated hospital stay of less than 4 weeks (28 days)
- Impaired lipid metabolism
- Severe hemorrhagic disorder. This is defined as platelets <50 K cells/uL, hemoglobin <7 g/dL, and INR >2.0. Patients treated with full therapeutic anticoagulation (i.e. for treatment of thrombosis) will also be excluded. This does not include patients on anticoagulants at prophylactic doses.
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- Unstable diabetes mellitus
- Collapse and shock
- Stroke/embolism
- Recent cardiac infarction
- Undefined coma status
- Allergy to egg or fish
- Prior treatment with Omegaven
- Liver disease (defined as elevated serum aminotransferases and/or direct bilirubin at the time of enrollment)
- Renal disease (defined as serum creatinine level above the normal range for age at the time of enrollment)
- Acid or base disorders (defined as serum bicarbonate less than 10 or greater than 40)
- Preterm infants less than 32 weeks gestation or birthweight <1500 grams who have not had a cranial ultrasound that showed no evidence of intraventricular hemorrhage at 36-40 weeks corrected gestational age
- Prior diagnosis of intraventricular hemorrhage
Who cannot join
None listed.
About this study
This is a randomized clinical trial comparing Omegaven® treatment with standard of care (soybean-based lipid formulation, Intralipid®) on bone health outcomes in infants with esophageal atresia (EA) undergoing surgical repair at Boston Children's Hospital.
Read the detailed description
Medical treatments and disease pathophysiology can result in prolonged immobilization that places hospitalized infants and children at risk for serious musculoskeletal complications including bone loss, fragility fractures, and muscle atrophy. Patients at the highest risk for inpatient fracture include premature infants, children with cerebral palsy, spinal cord injury, neuromuscular disorders (e.g., Duchenne Muscular Dystrophy or Spinal Muscular Atrophy), lengthy post-operative immobilization such as esophageal atresia (EA), and prolonged use of parenteral nutrition (PN). These fractures can result in significant discomfort, increase medical costs, may require surgical intervention, and may result in long term deleterious effects on musculoskeletal health.
Omega-3 polyunsaturated fatty acids (O3PuFA) are important bio-mediators modulating bone formation and remodeling. We demonstrated that O3PuFA provide protection of bone microstructure by increasing the number of trabecular elements and subsequently strengthening the trabecular network in young mice. Human studies suggest an association between O3PuFA intake and increased bone mineral density (BMD) in adults, and we also demonstrated decreased fracture risk in infants. O3PuFA may reduce bone resorption by modulating inflammatory cytokines and inhibiting osteoclast differentiation and activity, and may also increase bone formation by increasing osteoblast differentiation and activity, which may provide the explanation for the observed skeletal benefits.
In this study, we propose the use of intravenous O3PuFA (Omegaven® , Fresenius Kabi, Bad Hamburg Germany) administration for the prevention of musculoskeletal complications due to immobilization in infants. Boston Children's Hospital (BCH) has more than 15 years' experience with this O3PuFA product, having treated more than 250 infants and children. Omegaven is currently under review by the FDA for treatment of infants with PN-associated liver disease.
The proposed study is a randomized, double blind clinical trial using comparing Omegaven® administration to the current standard of care (soybean-based lipid formulation, Intralipid®) on musculoskeletal health in high risk infants with EA admitted at BCH. Infants with EA have been observed to have dramatic bone loss and a very high fracture rate (over 40%) related to their prolonged post-operative immobilization; therefore, these patients represent the ideal model to evaluate this intervention. By targeting this particular patient population at such high risk for musculoskeletal complications and limited confounding factors, the effects of our intervention will have the highest probability of being identified if such a benefit does exist.
In this pilot study, thirty-two infants with EA will be randomized to either treatment arm for a four-week treatment period. Safety outcomes will include regular laboratory monitoring as per routine standard of care. Efficacy outcomes will include (1) computed tomography (CT) of the bilateral distal femurs at baseline and at 4 weeks, which will provide skeletal outcomes including volumetric bone density, bone geometry, and bone strength estimates, (2) serum and urine markers of bone turnover, and (3) incidence of fracture in the post-operative period. All subjects will continue to receive treatments according to standard of care regardless of group assignment, including physical therapy, nutritionist consult, fracture precautions, and regular laboratory monitoring per discretion of the primary medical team.
- Conditions
- Esophageal Atresia
- Being tested
- Omegaven, Intralipid
- Medical subject headings
- Esophageal Atresia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
OmegavenDrug
Intravenous omega 3 fatty acid administration
IntralipidDrug
Standard of care
| Study group | Role | What they receive |
|---|---|---|
| Omegaven | Experimental | 15 infants with esophageal atresia undergoing surgical repair will receive Omegaven 1 g/kg/day IV infused over 8-24 hours for 28 days Receives: Drug: Omegaven |
| Intralipid | Active comparator | 15 infants with esophageal atresia undergoing surgical repair will receive the standard of care lipid formulation (Intralipid) as per hospital protocol for 28 days Receives: Drug: Intralipid |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in total volumetric bone mineral density of the distal femur
Computed tomography
Measured: Baseline and 28 days
Secondary outcomes (5)
Cortical and trabecular volumetric bone mineral density of the distal femur
Computed tomography
Measured: Baseline and 28 days
Bone geometry and bone strength estimates of the distal femur
Computed tomography
Measured: Baseline and 28 days
Bone turnover markers
Blood and urine testing
Measured: Baseline, 14 days, and 28 days
Incidence of fracture
Incidence of fracture
Measured: 28 days
Incidence of adverse events
Incidence of adverse events
Measured: Daily for 28 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Apr 2017
- Study startSep 2019 (estimated)
- Primary completionSep 2023 (estimated)
- Study completionSep 2023 (estimated)
Why it stopped: Lack of funding
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Esophageal AtresiaStudies of the same condition, open and under way.
- More trials run by Boston Children's HospitalThe 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boston Children's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Melissa Putman, Boston Children's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03127345
- Sponsor's protocol ID
- IRB-P00024279
- Status last verified
- Sep 2019
- First submitted
- 7 Apr 2017
- Last updated
- 16 Sep 2019
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Fallon EM, Nazarian A, Nehra D, Pan AH, O'Loughlin AA, Nose V, Puder M. The effect of docosahexaenoic acid on bone microstructure in young mice and bone fracture in neonates. J Surg Res. 2014 Sep;191(1):148-55. doi: 10.1016/j.jss.2014.04.005. Epub 2014 Apr 12.
PubMed 24793452Le HD, de Meijer VE, Robinson EM, Zurakowski D, Potemkin AK, Arsenault DA, Fallon EM, Malkan A, Bistrian BR, Gura KM, Puder M. Parenteral fish-oil-based lipid emulsion improves fatty acid profiles and lipids in parenteral nutrition-dependent children. Am J Clin Nutr. 2011 Sep;94(3):749-58. doi: 10.3945/ajcn.110.008557. Epub 2011 Jul 20.
PubMed 21775562Nehra D, Fallon EM, Potemkin AK, Voss SD, Mitchell PD, Valim C, Belfort MB, Bellinger DC, Duggan C, Gura KM, Puder M. A comparison of 2 intravenous lipid emulsions: interim analysis of a randomized controlled trial. JPEN J Parenter Enteral Nutr. 2014 Aug;38(6):693-701. doi: 10.1177/0148607113492549. Epub 2013 Jun 14.
PubMed 23770843
Study at a glance
From the registry record, last updated by the sponsor on 16 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Omega 3 Fatty Acid Treatment for Pediatric Musculoskeletal Health
- ClinicalTrials.gov ID
- NCT03127345
- Acronym / sponsor ID
- IRB-P00024279
- Conditions
- Esophageal Atresia
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Lack of funding
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Boston Children's HospitalUniversity, hospital or other
- Study start
- Sep 2019 (estimated)
- Primary completion
- Sep 2023 (estimated)
- Study completion
- Sep 2023 (estimated)
- First posted
- 25 Apr 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.
This is a randomized clinical trial comparing Omegaven® treatment with standard of care (soybean-based lipid formulation, Intralipid®) on bone health outcomes in infants with esophageal atresia (EA) undergoing surgical repair at Boston Children's Hospital.
Detailed description
Medical treatments and disease pathophysiology can result in prolonged immobilization that places hospitalized infants and children at risk for serious musculoskeletal complications including bone loss, fragility fractures, and muscle atrophy. Patients at the highest risk for inpatient fracture include premature infants, children with cerebral palsy, spinal cord injury, neuromuscular disorders (e.g., Duchenne Muscular Dystrophy or Spinal Muscular Atrophy), lengthy post-operative immobilization such as esophageal atresia (EA), and prolonged use of parenteral nutrition (PN). These fractures can result in significant discomfort, increase medical costs, may require surgical intervention, and may result in long term deleterious effects on musculoskeletal health.
Omega-3 polyunsaturated fatty acids (O3PuFA) are important bio-mediators modulating bone formation and remodeling. We demonstrated that O3PuFA provide protection of bone microstructure by increasing the number of trabecular elements and subsequently strengthening the trabecular network in young mice. Human studies suggest an association between O3PuFA intake and increased bone mineral density (BMD) in adults, and we also demonstrated decreased fracture risk in infants. O3PuFA may reduce bone resorption by modulating inflammatory cytokines and inhibiting osteoclast differentiation and activity, and may also increase bone formation by increasing osteoblast differentiation and activity, which may provide the explanation for the observed skeletal benefits.
In this study, we propose the use of intravenous O3PuFA (Omegaven® , Fresenius Kabi, Bad Hamburg Germany) administration for the prevention of musculoskeletal complications due to immobilization in infants. Boston Children's Hospital (BCH) has more than 15 years' experience with this O3PuFA product, having treated more than 250 infants and children. Omegaven is currently under review by the FDA for treatment of infants with PN-associated liver disease.
The proposed study is a randomized, double blind clinical trial using comparing Omegaven® administration to the current standard of care (soybean-based lipid formulation, Intralipid®) on musculoskeletal health in high risk infants with EA admitted at BCH. Infants with EA have been observed to have dramatic bone loss and a very high fracture rate (over 40%) related to their prolonged post-operative immobilization; therefore, these patients represent the ideal model to evaluate this intervention. By targeting this particular patient population at such high risk for musculoskeletal complications and limited confounding factors, the effects of our intervention will have the highest probability of being identified if such a benefit does exist.
In this pilot study, thirty-two infants with EA will be randomized to either treatment arm for a four-week treatment period. Safety outcomes will include regular laboratory monitoring as per routine standard of care. Efficacy outcomes will include (1) computed tomography (CT) of the bilateral distal femurs at baseline and at 4 weeks, which will provide skeletal outcomes including volumetric bone density, bone geometry, and bone strength estimates, (2) serum and urine markers of bone turnover, and (3) incidence of fracture in the post-operative period. All subjects will continue to receive treatments according to standard of care regardless of group assignment, including physical therapy, nutritionist consult, fracture precautions, and regular laboratory monitoring per discretion of the primary medical team.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Omegaven | Experimental | Drug: Omegaven15 infants with esophageal atresia undergoing surgical repair will receive Omegaven 1 g/kg/day IV infused over 8-24 hours for 28 days |
| Intralipid | Active comparator | Drug: Intralipid15 infants with esophageal atresia undergoing surgical repair will receive the standard of care lipid formulation (Intralipid) as per hospital protocol for 28 days |
Who may qualify
- Ages
- Up to 12 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (18 listed)
- 1) Diagnosis of long-gap EA (esophageal gap length >3cm) 2) Age <12 months (not yet reached 12 month birthday) 3) Anticipated surgical repair for management of EA utilizing esophageal traction requiring prolonged intubation, muscle relaxation, and parenteral nutrition dependence.
- Known genetic bone disease, including osteogenesis imperfecta, idiopathic infantile hypercalcemia, and vitamin D resistant rickets
- Prior fragility fracture (including humerus or femur)
- Anticipated hospital stay of less than 4 weeks (28 days)
- Impaired lipid metabolism
Key exclusion criteria (0 listed)
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 |
|---|---|---|
| OmegavenIntravenous omega 3 fatty acid administration | Drug | Omegaven |
| IntralipidStandard of care | Drug | Intralipid |
Primary outcome
Change in total volumetric bone mineral density of the distal femur
Time frame: Baseline and 28 days
Computed tomography
5 secondary outcomes
Cortical and trabecular volumetric bone mineral density of the distal femur
Time frame: Baseline and 28 days
Bone geometry and bone strength estimates of the distal femur
Time frame: Baseline and 28 days
Bone turnover markers
Time frame: Baseline, 14 days, and 28 days
Incidence of fracture
Time frame: 28 days
Incidence of adverse events
Time frame: Daily for 28 days
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Sep 2019.
- Background: PubMed 24793452Fallon EM, Nazarian A, Nehra D, Pan AH, O'Loughlin AA, Nose V, Puder M. The effect of docosahexaenoic acid on bone microstructure in young mice and bone fracture in neonates. J Surg Res. 2014 Sep;191(1):148-55. doi: 10.1016/j.jss.2014.04.005. Epub 2014 Apr 12.
- Background: PubMed 21775562Le HD, de Meijer VE, Robinson EM, Zurakowski D, Potemkin AK, Arsenault DA, Fallon EM, Malkan A, Bistrian BR, Gura KM, Puder M. Parenteral fish-oil-based lipid emulsion improves fatty acid profiles and lipids in parenteral nutrition-dependent children. Am J Clin Nutr. 2011 Sep;94(3):749-58. doi: 10.3945/ajcn.110.008557. Epub 2011 Jul 20.
- Background: PubMed 23770843Nehra D, Fallon EM, Potemkin AK, Voss SD, Mitchell PD, Valim C, Belfort MB, Bellinger DC, Duggan C, Gura KM, Puder M. A comparison of 2 intravenous lipid emulsions: interim analysis of a randomized controlled trial. JPEN J Parenter Enteral Nutr. 2014 Aug;38(6):693-701. doi: 10.1177/0148607113492549. Epub 2013 Jun 14.
- Individual participant dataSharing planned: Undecided
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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.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Omegaven and Intralipid in people with Esophageal Atresia, run by Boston Children's Hospital.
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 18 inclusion and 0 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: withdrawn, as of the sponsor's last update on 16 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.
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.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
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?
Change in total volumetric bone mineral density of the distal femur (time frame: Baseline and 28 days). 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 NCT03127345, which also lists 3 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 16 Sep 2019.