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The effect of Resveratrol on the expression of the granulosa apoptosis-associated genes in polycystic ovary syndrome and its relationship with in vitro fertilization outcome

The effect of Resveratrol on the expression of the granulosa apoptosis-associated genes in polycystic ovary syndrome and its relationship with in vitro fertilization outcome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200905048630N1
Enrollment
40
Registered
2020-09-21
Start date
2020-12-21
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

polycystic ovarian syndrome: PCOS. polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group: from the beginning of the cycle, individuals in this group will receive one 99% pure trans-Resveratrol capsule (800 mg per day) as orally purchased from the US co

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Women with polycystic ovary syndrome based on Rotterdam criteria Women of childbearing age between 18 and 40 years Candidate for in vitro fertilization Not receiving insulin

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Apoptosis. Timepoint: 40 days after the beginning of the intervention. Method of measurement: real time pcr.

Secondary

MeasureTime frame
Egg numbers. Timepoint: 40 days after the beginning of the intervention. Method of measurement: Counting.;Number of embryos. Timepoint: 43 days after the beginning of the intervention. Method of measurement: Counting.;Number of good quality embryo. Timepoint: 43 days after the beginning of the intervention. Method of measurement: Counting.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEnsieh salehi

Bandare-abbas University of Medical Sciences

salehiensieh@gmail.com+98 76 3333 0755

Outcome results

None listed

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