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Fish Oil Supplementation to Pregnant Women in China (FOPCHIN)

Primary Purpose

Premature Birth

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
High dose fish oil
Low dose fish oil
Olive oil
Sponsored by
Centre for Fetal Programming, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Premature Birth focused on measuring fish oil, preterm birth, pregnancy, China, prevention

Eligibility Criteria

20 Years - 44 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Pregnancy without known complications

Exclusion Criteria:

  • Regular user of fish oil
  • Regular user of NSAIDs
  • Known twin pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Placebo Comparator

    Arm Label

    High dose fish oil

    Low dose fish oil

    Control

    Arm Description

    Women will be offered 4 capsules per day containing fish oil

    Women will be offered 4 capsules per day containing mixed fish oil and olive oil

    Women will be offered 4 capsules per day containing olive oil

    Outcomes

    Primary Outcome Measures

    Premature birth
    Delivery occurring earlier than 259 gestation days

    Secondary Outcome Measures

    Full Information

    First Posted
    May 11, 2016
    Last Updated
    May 11, 2016
    Sponsor
    Centre for Fetal Programming, Denmark
    Collaborators
    Shanghai Institute of Planned Parenthood Research
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02770456
    Brief Title
    Fish Oil Supplementation to Pregnant Women in China
    Acronym
    FOPCHIN
    Official Title
    Fish Oil Supplementation to Prevent Preterm Delivery in China: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2008 (undefined)
    Primary Completion Date
    December 2015 (Actual)
    Study Completion Date
    April 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Centre for Fetal Programming, Denmark
    Collaborators
    Shanghai Institute of Planned Parenthood Research

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This randomized controlled trial with fish oil supplementation to pregnant women conducted in areas of China, which are generally low in fish intake and low income, aims at answering the following primary questions: Is a dose of 2.0 g/d long chain n-3 fatty acids efficient in preventing preterm birth Is a dose of 0.5 g/d long chain n-3 fatty acids efficient in preventing preterm birth Is a dose of 0.5 g/d as efficient as a dose of 2.0 g/d in affecting timing of spontaneous delivery in the preterm period
    Detailed Description
    The basic design is that of a randomized controlled trial with three groups randomized in ratios of 1:1:1. Two different doses of long chain n-3 fatty acids are tested against zero grams long chain n-3 fatty acids (lc-n3FA). These are provided in similarly looking gelatine capsules with either fish oil, a mixture (1:3) of fish oil and olive oil, or olive oil. Eligible women are randomized at around gestation weeks 16-24 and are asked to take the capsules until they have completed the preterm period (i.e. at 37 full gestation weeks) or until they deliver. Women are asked to complete questionnaires at randomization about diet and other baseline information, and again in gestation week 30 and after delivery. The trial is undertaken at hospitals in the two provinces of Gan-Su and Shaanxi. The three randomization groups will be compared with respect to proportions of preterm delivery. Cox regression will be used to compare the groups with respect to rates of spontaneous deliveries while accounting for elective delivery by regarding these as censoring events.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Premature Birth
    Keywords
    fish oil, preterm birth, pregnancy, China, prevention

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    5531 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    High dose fish oil
    Arm Type
    Experimental
    Arm Description
    Women will be offered 4 capsules per day containing fish oil
    Arm Title
    Low dose fish oil
    Arm Type
    Experimental
    Arm Description
    Women will be offered 4 capsules per day containing mixed fish oil and olive oil
    Arm Title
    Control
    Arm Type
    Placebo Comparator
    Arm Description
    Women will be offered 4 capsules per day containing olive oil
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    High dose fish oil
    Intervention Description
    Four 0.72-gram gelatine capsules per day with fish oil providing 2.0 g/d lc-n3FA
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Low dose fish oil
    Intervention Description
    Four 0.72-gram gelatine capsules per day with a mixture of fish oil and olive oil providing 0.5 g/d lc-n3FA
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Olive oil
    Intervention Description
    Four 0.72-gram gelatine capsules per day with olive oil providing 0 g/d lc-n3FA
    Primary Outcome Measure Information:
    Title
    Premature birth
    Description
    Delivery occurring earlier than 259 gestation days
    Time Frame
    20 weeks on average, from randomization at gestation weeks 16-24 until on average gestation week 40

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    44 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Pregnancy without known complications Exclusion Criteria: Regular user of fish oil Regular user of NSAIDs Known twin pregnancy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Sjurdur F Olsen, Ph.D.
    Organizational Affiliation
    Statens Serum Institut
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Weijin Zhou, Ph.D.
    Organizational Affiliation
    Shanghai Institute of Planned Parenthood Research
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    Citations:
    PubMed Identifier
    31387119
    Citation
    Olsen SF, Halldorsson TI, Li M, Strom M, Mao Y, Che Y, Wang Y, Duan F, Olsen J, Zhou W. Examining the Effect of Fish Oil Supplementation in Chinese Pregnant Women on Gestation Duration and Risk of Preterm Delivery. J Nutr. 2019 Nov 1;149(11):1942-1951. doi: 10.1093/jn/nxz153. Erratum In: J Nutr. 2019 Nov 1;149(11):2073.
    Results Reference
    derived

    Learn more about this trial

    Fish Oil Supplementation to Pregnant Women in China

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