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Effect of vitamin E, vitamin D on treatment of infertility in PCOS patients

Evaluation of the effect of supplementation with vitamin E and vitamin D on serum and follicular fluid oxidative and anti oxidative stress factors, oocyte quality and ICSI outcomes in PCOS infertile women candidate for ICSI who referred to Infertility Clinic of Avicenna Research Center during 2014-2015

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081018662N1
Enrollment
100
Registered
2014-08-21
Start date
2014-08-23
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

Condition 1: Polycystic ovarian syndrome. Condition 2: Infertility. Sclerocystic ovary syndromeStein-Leventhal syndrome In vitro fertilization

Interventions

Intervention 1: placebo of vit E once daily for 2 months. Intervention 2: pearl vit D,Biweekly for 2 months. Intervention 3: placebo of vit D,biweekly for 2 months. Intervention 4: pearl vit E,400 IU
Treatment - Drugs
placebo of vit E once daily for 2 months
pearl vit D,Biweekly for 2 months
placebo of vit D,biweekly for 2 months
pearl vit E,400 IU,once daily for 2 months

Sponsors

Avicenna Infertility Clinic
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 38 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: PCOS patients based on ROTERDOM criteria; age:18-38 years old; day3 FSH level less than 12; BMI:20-34. Exclusion criteria: patients with heart, liver or renal disease; patients with Endometriosis; use of anticoagulats: ASA, Heparin, Warfarin; use of antidepresants:Fluoxetin, Certeralin; use of Statins: Levastatin, Atorvastatin; patients with Eye disease: Retinitis pigmentosa; use of anti inflammatory drugs and corticosteroids:prednisolon; use of vitamins and anti oxidants in 3 months ago; vit K deficiency and bleeding disorders; history of chemotherapy or radiotherapy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum malondealdehyde. Timepoint: before intervention and after intervention on the oocyte collection day. Method of measurement: American key man kit.;Serum total antioxidant capaity(TAC). Timepoint: before intervention and after intervention on the oocyte collection day. Method of measurement: American key man kit.;Serum super oxid dismuthase. Timepoint: before intervention and after intervention on the oocyte collection day. Method of measurement: American key man kit.;Follicular fluid malondealdehyde. Timepoint: on the oocyte collection day. Method of measurement: American key man kit.;Follicular fluid total anti oxidant capacity. Timepoint: on the oocyte collection day. Method of measurement: American key man kit.;Follicular fluid super oxid dismuthase. Timepoint: on the oocyte collection day. Method of measurement: American key man kit.

Secondary

MeasureTime frame
Oocyte quality. Timepoint: on the day of oocyte collection. Method of measurement: morphologic assesment with microscope.;ICSI outcome. Timepoint: 2 weeks after embryo transfer. Method of measurement: serum BHCG.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farnaz Fatemi

Avicenna Infertility Clinic

f.fatemi@avicenna.ac.ir+98 21 23519

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 11, 2026