Cholestasis Prevention: Efficacy of IV Fish Oil
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02115
- Childrens's Hospital Boston
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria (all of the following):
- Congenital or acquired gastrointestinal disease requiring surgical intervention [such as Midgut volvulus, Gastroschisis-(with known or suspected atresia(s), perforation(s) requiring a jejunostomy, or bowel resections > 20cm), Omphalocele, Jejunal atresia or NEC-(no peritoneal drains) or duodenal atresia] ; and
- Expected dependence on parenteral nutrition for full or partial nutritional support for an anticipated duration of therapy of at least 21 days; Subjects will be judged by their clinical team to require PN support a minimum of 21 days based on the following criteria: inability to tolerate enteral feedings, lack of audible bowel sounds, contraindications to initiation of enteral feedings (e.g., grossly bloody stools or other sign of intestinal ischemia, hypotension, bilious emesis, or clinical or radiographic evidence of bowel obstruction); and
- Neonates and infants < 3 months of age (postnatally); and
- Gestational age > 28 weeks; and
- Baseline direct bilirubin less than 1.0 mg/dL (normal); and
- Weight > 1 kg
Exclusion criteria(any one of the following):
- Exposure to soybean oil fat emulsion for greater than three weeks (>21 days) at time of enrollment
- Known or suspected intolerance or allergy to any of the components of the study IFE, including fish, soy or egg protein
- Inability to obtain written informed consent prior to the baseline labs
- The patient is enrolled in any other clinical trial involving an investigational agent (unless approved by the designated physicians on the multidisciplinary team)
- Intention to transfer care to another patient facility within 3 months of baseline labs
- Any serum triglyceride level greater than 400 mg/dL at baseline
- History of severe hemolytic disorders or INR greater than 1.5 at baseline (INR cutoff of greater than 2 for babies less than 1 week of age)
- History of shock requiring vasopressors (dopamine equal or less than 20 micrograms/kilogram/minute is allowed; all other use of vasopressors is excluded)
- Preexisting liver disease, regardless of etiology
- Hemodynamically unstable as judged by PI
- Renal failure (creatinine greater than 0.4 mg/dL unless less than 1 month of age-then at the PI's discretion)
- Patient previously had STEP (Serial Transverse Enteroplasty Procedure)
- Patient is currently on ECMO or nitric oxide
- GGTP > 80 mg/L at baseline
- Weight < 1 kg at time of enrollment
- Gestational age < 28 weeks at time of enrollment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: QUADRUPLE
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
EXPERIMENTAL: Omegaven
Omegaven is a fish based intravenous fat emulsion
|
Omegaven is a fish based intravenous fat emulsion
|
|
ACTIVE_COMPARATOR: Intralipid
|
Intralipid is a plant based intravenous fat emulsion
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Presence vs. absence of PN-associated cholestasis (PNAC)
Time Frame: 6 months
|
The definition of "Presence vs. Absence of PNAC" will vary with the post conceptual age of the child.
In infants > 40 weeks post conceptual age, we will define PN-associated cholestasis as four consecutive measurements (> 6 days apart) of serum direct bilirubin > 2.0mg/dL obtained over a 30 day period in the absence of other demonstrable etiologies of cholestasis.
Due to hepatic immaturity, for infants < 40 weeks post conceptual age, PN associated cholestasis will be defined as four consecutive measurements (> 6 days apart) of serum direct bilirubin > 2.0mg/dL obtained over a 42 day period.
|
6 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fatty acid profiles
Time Frame: 6 months
|
(i.e., Mead acid levels, triene:tetraene ratios, total omega-3 and omega-6 fatty acid levels, arachidonic acid levels)
|
6 months
|
|
Weight and height gain
Time Frame: 6 months
|
6 months
|
|
|
Liver function tests
Time Frame: 6 months
|
(i.e.
serum triglycerides, cholesterol, ALT, AST and total and direct bilirubin levels)
|
6 months
|
|
Death from PNALD liver or liver/gastrointestinal tract transplant.
Time Frame: 1 year
|
1 year
|
|
|
Duration of parenteral nutrition
Time Frame: 6 months
|
(i.e.
enteral feeding tolerance, including days to reach full enteral feeding (approximately 100-125kcal/kg/d + 10%) after randomization and the number of episodes of feeding intolerance (defined as an interruption of enteral feedings for > 12 hrs) , number of infants requiring TPN providing > 10% of total daily fluid volume at 12 weeks after randomization, and duration of TPN providing > 10% of total daily fluid intake)
|
6 months
|
|
Frequency of blood stream infections
Time Frame: 6 months
|
6 months
|
|
|
Inflammatory markers (C-reactive protein), cytokine levels
Time Frame: 6 months
|
6 months
|
|
|
Incidence and severity of ROP
Time Frame: 6 months
|
6 months
|
|
|
Neurodevelopment Assessments
Time Frame: 6, 12, & 24 months (corrected for gestational age)
|
Neurodevelopment will be assessed at 6, 12, and 24 months (corrected) using Bayley Scales of Infant Development III(mean total, cognitive, language, and motor scaled score; and frequency of each score <70).
The MSD parent questionnaire will be mailed at 12 and 24 months (corrected); and the Parent Report of Children's Abilities - Revised (PARCA-R) parent questionnaire will be mailed at 24 months (coorected).
|
6, 12, & 24 months (corrected for gestational age)
|
Collaborators and Investigators
Sponsor
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (ACTUAL)
Primary Completion
Study Completion (ACTUAL)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
First Posted
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 06-03-0105
- 1R01FD003436-01 (FDA)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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