Skip to content

"Survey of the Effect of Omega-3 in the Prevention of Preeclampsia”

Survey of the Effect of Omega-3 in the Prevention of Preeclampsia in Pregnant Women Suffering Hyperlipidemia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210426051094N1
Enrollment
72
Registered
2021-06-07
Start date
2021-05-02
Completion date
Unknown
Last updated
2021-06-21

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

Conditions

Preeclampsia in Pregnant Women Suffering Hyperlipidemia.

Interventions

Intervention 1: Intervention group: From the first month to the end of pregnancy for 9 months, the intervention group receives omega-3 daily as one gram capsule containing eicosapentalenoic acid and d

Sponsors

Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Pregnant Women Suffering Hyperlipidemia that triglyceride levels is above 150 Milligrams per Deciliter.

Exclusion criteria

Exclusion criteria: Pregnant women that are suffering metabolic diseases. Pregnant women that have the age of less than 20 years and over the age of 40 years. Pregnant women that have a history of preeclampsia in a previous pregnancy or in a first-degree relative. Pregnant women that have a history of having twins. Pregnant women that have a body mass index equal to or greater than 29. Pregnant women that have kidney disease, high blood pressure, diabetes and hyperthyroidism. Pregnant women that use of aspirin, calcium, anticoagulants and insulin. Pregnant women that do not have history of omega-3 allergies.

Design outcomes

Primary

MeasureTime frame
Preeclampsia. Timepoint: Before the intervention in the first month of pregnancy and 9 months after the intervention in the last month of pregnancy. Method of measurement: Blood pressure above 140 to 90 mm Hg, swelling of the hands and face, overweight, based on the results of clinical trials of the patient's blood, including protein in the urine, increased liver enzymes, decreased platelet count, increased creatine and ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Mahdavian Naghash Zargar

Kurdistan University of Medical Sciences

mnz_shima@yahoo.com+98 87 3366 0089

Outcome results

None listed

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