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The effect of fish-oil supplementation on lipid profile of pregnant mothers: a randomized controlled trial

The effect of fish-oil supplementation on lipid profile of pregnant mothers: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015070523067N1
Enrollment
150
Registered
2015-08-13
Start date
2014-11-27
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lipid levels in Pegnant women. Other obstetric conditions, not elsewhere classified

Interventions

Intervention 1: Group interventions: fish oil capsules (containing 120 mg of DHA and 180 mg, 1000 mg EPA) ,Every day 1 number. Intervention 2: Control group: placebo (same shape, size and weight with
Treatment - Drugs
Placebo
Group interventions: fish oil capsules (containing 120 mg of DHA and 180 mg, 1000 mg EPA) ,Every day 1 number
Control group: placebo (same shape, size and weight with other capsules ,Every day 1 number

Sponsors

Endocrine Research Center, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to participate in the study, aged 18-35 years, first to fifth pregnancy, pregnant women with 16-20weeks of gestation, single pregnancy; BMI less than 30, healthy pregnant women with no previous underlying medical condition, including heart disease, kidney, gastrointestinal, respiratory, autoimmune, diabetes, impaired glucose tolerance testing in the current pregnancy, thyroid, epilepsy, hypertension underlying psychiatric disorders, hyperlipidemia and not to use any drugs because of the above conditions .Exclusion criteria:, bleeding, placenta previa, placenta detachment in current pregnancy, infertility and premature labor history, the existence of any history of allergy to fish or fish oil or other products or allergic to gelatin, the unfortunate incident that had occurred 6 months prior to the study, smoking or drugs, bleeding disorders or taking anticoagulants, participating in another study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Lipid Profile. Timepoint: begiining of study,fifth care of pregnancy. Method of measurement: blood analysis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Aslani

Tabriz University of Medical Sciences

hosseinaslani1990@gmail.com+98 41 3382 3655

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026