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The effect of omega3 supplementation in preeclampsia in pregnant women at risk in Qazvin

The effect of omega3 supplementation in preeclampsia in pregnant women at risk in Qazvin

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138706061113N1
Enrollment
100
Registered
2010-03-27
Start date
2007-09-23
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

Preeclampsia. Gestational [pregnancy-induced] hypertension with significant proteinuria

Interventions

Intervention 1: Omega-3, 1gram for 24 weeks. Intervention 2: Placebo for 24 weeks.
Treatment - Drugs
Placebo
Omega-3, 1gram for 24 weeks
Placebo for 24 weeks

Sponsors

Qazvin University of Medical Sciences, Zahravi drug company
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women whose gestational age is between 14 to 18 weeks and are ready to cooperate, being high risk for preeclampsia (first gravidy, under the age of 20 and over 40, a history of preeclampsia during the previous gravidy or immediate member of family, BMI more than 29, history of twin fetuses); Inclusion criteria: consumption of Aspirin, Calcium, anticoagulants, allergy to omega3 or fish, presence digestive diseases which need to treatment,

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hypertention. Timepoint: Every 4 hours. Method of measurement: determination of BP by the auscullatory method.;Proteinuria. Timepoint: daily. Method of measurement: Urine Protein.

Secondary

MeasureTime frame
Level of liver enzymes. Timepoint: daily. Method of measurement: laboratory.;Headache. Timepoint: Every 4 hours. Method of measurement: Asking from patients.;Thrombocytopenia. Timepoint: daily. Method of measurement: laboratory.;Abdominal pain. Timepoint: Every 4 hours. Method of measurement: Asking from pateints.;Vision problems. Timepoint: Every 4 hours. Method of measurement: Asking from patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Ranjkesh

nursing and midwifery school

franjkesh@qums.ac.ir+98 28 1377 4540

Outcome results

None listed

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