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Effect of Omega 3 supplementation in women with polycystic ovary syndrome

Effect of Omega3 supplementation on Visfatin, Adiponectin, and Anthropometric indices in women with polycystic ovary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012071410281N1
Enrollment
64
Registered
2012-09-09
Start date
2012-06-21
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

polycystic ovary syndrome. Sclerocystic ovary syndrome Stein-Leventhal syndrome

Interventions

Intervention 1: intervention:capsules of fish-oil (3 g/d) for 2 month. Intervention 2: placebos of fish-oil (3 g/d) for 2 month.
Placebo
intervention:capsules of fish-oil (3 g/d) for 2 month
placebos of fish-oil (3 g/d) for 2 month

Sponsors

Institute for Reproductive Sciences, Research and clinical Center for Infertility
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: criteria inclusion: females 20-40years; PCOS diagnostic according to Roterdam criteria; BMI>25; No history about intake of any drug during the last 3 months that may affect the insulin sensitivity or hormonal profile such as: oral contraceptives, glucocorticoids, ovulation induction agents, anti diabetic and anti obesity drugs, estrogenic, antiandrogenic or anti hypertensive medication; Not being in any diet in the last 3month; Do not have any addiction to tobacco and alcohol; Do not taking a Omega-3 supplement in the last 3 month; Do not be menopause; Do not use anti-coagulant medicine; Do not use anti-depression medication; Do not be diabetic and hypothyroidism. exclusion criteria: Essentially needs for intake of OCP to treatment; Do not will to be in the study; Do not obey the Protocols of the study and do not digest more than 20% of supplements.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum visfatin-. Timepoint: before and after intervention. Method of measurement: visfatin ng/ml Elisa kit-.;Serum adiponectin. Timepoint: before and after intervention. Method of measurement: adiponectin Elisa kit µg/ml-.;Serum LH. Timepoint: before and after intervention. Method of measurement: LH Elisa kit U/l.;Serum FSH. Timepoint: before and after intervention. Method of measurement: FSHElisa kit U/l-.;Serum Prolactin. Timepoint: before and after intervention. Method of measurement: prolactin Elisa ng/mL.;Body weight. Timepoint: before and after intervention. Method of measurement: leveled platform scale.;BMI-. Timepoint: before and after intervention. Method of measurement: leveled platform scale-stadiometer.;Waist circumference. Timepoint: before and after intervention. Method of measurement: tape.;Hip circumference. Timepoint: before and after intervention. Method of measurement: tape.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoorieh Daneshbodi

Shahid sadoughi university of medical sciences and health services

h_daneshbodi@ssu.ac.ir+98 35 1824 7085

Outcome results

None listed

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