A Fatty Acids Study in Preventing Retinopathy of Prematurity (DonnaMega)
Primary Purpose
Retinopathy of Prematurity
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
SMOFlipid
Clinoleic
Sponsored by
About this trial
This is an interventional prevention trial for Retinopathy of Prematurity focused on measuring Retinopathy of Prematurity, Preterm, Fatty acids
Eligibility Criteria
Inclusion Criteria:
- Signed informed consent from parents/guardians;
- Subject must be below 28 weeks of gestation
Exclusion Criteria:
- Detectable clinical gross malformation;
- Known or suspected chromosomal abnormality, genetic disorder, or syn-drome, according to the investigator's opinion;
- Clinically significant neuropathy, nephropathy, retinopathy, or other micro- or macrovascular disease requiring treatment, according to the investigator's opinion;
- Any other condition or therapy that, in the investigator's opinion, may pose a risk to the subject or interfere with the subject's ability to be compliant with this protocol or interfere with interpretation of results.
- Bleeding disorder.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Clinoleic
SMOFlipid
Arm Description
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Outcomes
Primary Outcome Measures
Retinopathy of Prematurity
We intend to analyze the content of Fatty Acids and correlate to Retinopathy of Prematurity development and interventional treatment. Analyze of phospholipids can be done on small amounts of blood, is relatively insensitive to short term fluctuations in intake and mirror the composition of many membranes in the body. The analyses will be made using gas-liquid chromatography. The method has a coefficient of variability of 1-3% for the Fatty Acids concerned.
Secondary Outcome Measures
Brain Growth
Cranial ultrasound will be performed according to clinical praxis. MRI of the brain will be performed at 40 weeks postmenstrual age (PMA) and correlated to interventional treatment.
Length in cm
Length in cm given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Weight in gram
Weight in gram given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Head circumference in cm
Head circumference in cm given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Full Information
NCT ID
NCT02760472
First Posted
March 30, 2016
Last Updated
April 29, 2016
Sponsor
Carola Pfeiffer-Mosesson
1. Study Identification
Unique Protocol Identification Number
NCT02760472
Brief Title
A Fatty Acids Study in Preventing Retinopathy of Prematurity
Acronym
DonnaMega
Official Title
A Randomised Intervention Single Center Study to Determine the Role of Fatty Acids in Serum in Preventing Retinopathy of Prematurity
Study Type
Interventional
2. Study Status
Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Carola Pfeiffer-Mosesson
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Most fatty acids, important for development and especially the Omega-3 fatty acids for the brain development are transferred in the third trimester with means that in the premature infant this transport via the placenta is interrupted and the infant is dependent on the concentrations in breast milk which vary depending on the mother's diet and her stores. It has even been suggested that low Omega-3 would be a cause of premature delivery. Many countries have much higher levels of Omega-3 fatty acids in breast milk than found in Sweden and breast milk substitutions are generally now supplemented with the Long Chained Poly Unsaturated Fatty Acids (LCPUFA). Therefore the supplementation to be given can not be seen to give any risks for the infant. On the contrary, several studies have shown that mother who eat equal to or less than twice fish a week during pregnancy give birth to infants with impaired development.
Low Omega-3 levels in premature infants between gestational ages of 23 and 40 weeks can be one reason for Retinopathy of Prematurity (ROP) development. Restoration of Omega-3, Dokosahexaenacid (DHA) and Eikosapentaenacid (EPA) to normal in utero levels may prevent ROP by allowing normal vessel growth and survival. An increase of Omega-3 levels bringing levels to within physiological range may prevent development of ROP.
Detailed Description
The study is a Randomised Intervention, Single-Center Study to Determine the Role of Fatty Acids in Serum and Breast Milk in preventing Retinopathy of Prematurity.
Subjects who meet all inclusion and none of the exclusion criteria will be enrolled into the study. Upon entry into the study, subjects will be randomized and given a unique subject number.
A randomised intervention study of 45+45 infants without major malformations born with a gestational age less than 28 weeks + 0 days will be performed.
Randomization of the patients to either:
Conventional fatty acid supplementation regime with Clinoleic (with Vitalipid infant and Soluvit supplementation) to the preterm infant
Or
SMOFlipid, (soybean oil, medium chain triglycerides, olive oil and fish oil),(with Vitalipid infant and Soluvit supplementation), where the quotient of Omega 6:3 is 2.5:1 in order to mimic the physiologic relation of fatty acids in cord blood from birth, to the preterm infant.
Thus there is one group of infants (n=45) that will receive Omega-3 in the fatty acid supplementation.
The time on parenteral nutrition and the amount of fatty acids given will be according to clinical routines.
The randomization of the patients will be performed by the controller of the study. Randomization will be in blocks with 10 children in each block.
Data collection
After the investigators have received informed consent from the parents/guardians, blood samples 0.2 ml from the child will be taken according to present clinical practice at if possible from cord (2ml) and at days 0, 7, 14, 28 and in postmenstrual weeks 32, 36 and 40. Blood samples from the mothers for Fatty Acids analyses will be taken after birth, day 7 and at gestational weeks 36 and 40. At the same time (except from day 1), breast milk samples are taken. Length in cm, weight in gram and head circumference in cm are measured weekly.
Screening for ROP will be performed, at least once a week, according to clinical routines using a specific protocol.
The investigators intend to analyze the content of phospholipids which can be done on small amounts of blood, is relatively insensitive to short term fluctuations in intake and mirror the composition of many membranes in the body. The analyses will be made using gas-liquid chromatography. The method has a coefficient of variability of 1-3% for the Fatty Acids concerned.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinopathy of Prematurity
Keywords
Retinopathy of Prematurity, Preterm, Fatty acids
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Clinoleic
Arm Type
Active Comparator
Arm Description
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Arm Title
SMOFlipid
Arm Type
Experimental
Arm Description
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Intervention Type
Drug
Intervention Name(s)
SMOFlipid
Intervention Description
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Intervention Type
Drug
Intervention Name(s)
Clinoleic
Intervention Description
Parenteral fatty acid supplementation to preterm infants in preventing retinopathy of prematurity
Primary Outcome Measure Information:
Title
Retinopathy of Prematurity
Description
We intend to analyze the content of Fatty Acids and correlate to Retinopathy of Prematurity development and interventional treatment. Analyze of phospholipids can be done on small amounts of blood, is relatively insensitive to short term fluctuations in intake and mirror the composition of many membranes in the body. The analyses will be made using gas-liquid chromatography. The method has a coefficient of variability of 1-3% for the Fatty Acids concerned.
Time Frame
When the retina is fully vascularised,i.e. at approximately 40 postmenstrual weeks.
Secondary Outcome Measure Information:
Title
Brain Growth
Description
Cranial ultrasound will be performed according to clinical praxis. MRI of the brain will be performed at 40 weeks postmenstrual age (PMA) and correlated to interventional treatment.
Time Frame
At 40 postmenstrual weeks and at 2.5 and 6 years.
Title
Length in cm
Description
Length in cm given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Time Frame
At 40 postmenstrual weeks and at 2.5 and 6 years.
Title
Weight in gram
Description
Weight in gram given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Time Frame
At 40 postmenstrual weeks and at 2.5 and 6 years.
Title
Head circumference in cm
Description
Head circumference in cm given in absolute values and in standard deviation scores, at 40 weeks postmenstrual age (PMA) and at 2.5 and 6 years will be correlated to interventional treatment.
Time Frame
At 40 postmenstrual weeks and at 2.5 and 6 years.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
23 Weeks
Maximum Age & Unit of Time
28 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Signed informed consent from parents/guardians;
Subject must be below 28 weeks of gestation
Exclusion Criteria:
Detectable clinical gross malformation;
Known or suspected chromosomal abnormality, genetic disorder, or syn-drome, according to the investigator's opinion;
Clinically significant neuropathy, nephropathy, retinopathy, or other micro- or macrovascular disease requiring treatment, according to the investigator's opinion;
Any other condition or therapy that, in the investigator's opinion, may pose a risk to the subject or interfere with the subject's ability to be compliant with this protocol or interfere with interpretation of results.
Bleeding disorder.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carola Pfeiffer-Mosesson, RN
Organizational Affiliation
The Queen Silvia Children's Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Yes
Citations:
PubMed Identifier
33004691
Citation
Cakir B, Hellstrom W, Tomita Y, Fu Z, Liegl R, Winberg A, Hansen-Pupp I, Ley D, Hellstrom A, Lofqvist C, Smith LE. IGF1, serum glucose, and retinopathy of prematurity in extremely preterm infants. JCI Insight. 2020 Oct 2;5(19):e140363. doi: 10.1172/jci.insight.140363.
Results Reference
derived
PubMed Identifier
32588218
Citation
Nilsson AK, Pedersen A, Malmodin D, Lund AM, Hellgren G, Lofqvist C, Pupp IH, Hellstrom A. Serum choline in extremely preterm infants declines with increasing parenteral nutrition. Eur J Nutr. 2021 Mar;60(2):1081-1089. doi: 10.1007/s00394-020-02312-2. Epub 2020 Jun 25.
Results Reference
derived
PubMed Identifier
30297879
Citation
Lundgren P, Hellgren G, Pivodic A, Savman K, Smith LEH, Hellstrom A. Erythropoietin serum levels, versus anaemia as risk factors for severe retinopathy of prematurity. Pediatr Res. 2019 Aug;86(2):276-282. doi: 10.1038/s41390-018-0186-6. Epub 2018 Sep 18.
Results Reference
derived
PubMed Identifier
29423508
Citation
Lofqvist CA, Najm S, Hellgren G, Engstrom E, Savman K, Nilsson AK, Andersson MX, Hard AL, Smith LEH, Hellstrom A. Association of Retinopathy of Prematurity With Low Levels of Arachidonic Acid: A Secondary Analysis of a Randomized Clinical Trial. JAMA Ophthalmol. 2018 Mar 1;136(3):271-277. doi: 10.1001/jamaophthalmol.2017.6658. Erratum In: JAMA Ophthalmol. 2018 Sep 1;136(9):1078.
Results Reference
derived
Links:
URL
http://www.rop.gu.se
Description
Homepage
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A Fatty Acids Study in Preventing Retinopathy of Prematurity
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