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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
Carola Pfeiffer-Mosesson
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Retinopathy of Prematurity focused on measuring Retinopathy of Prematurity, Preterm, Fatty acids

Eligibility Criteria

23 Weeks - 28 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Signed informed consent from parents/guardians;
  2. Subject must be below 28 weeks of gestation

Exclusion Criteria:

  1. Detectable clinical gross malformation;
  2. Known or suspected chromosomal abnormality, genetic disorder, or syn-drome, according to the investigator's opinion;
  3. Clinically significant neuropathy, nephropathy, retinopathy, or other micro- or macrovascular disease requiring treatment, according to the investigator's opinion;
  4. 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.
  5. 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

    First Posted
    March 30, 2016
    Last Updated
    April 29, 2016
    Sponsor
    Carola Pfeiffer-Mosesson
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    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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