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The effects of Resveratrol on PCOS.

The effects of Resveratrol on expression of some ER stress pathway genes in granulosa cells and some circulating inflammatory markers in PCOS patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016041827453N1
Enrollment
40
Registered
2016-05-25
Start date
2016-05-04
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 ovarian syndrome (PCOS). Polycystic ovarian syndrome

Interventions

Intervention 1: For Intervention Group: Resveratrol (manufactured by Biovita company), Orally 1gr/day (2 Cap.) for 40 days from the beginning of the menstruation cycle till oocyte retrieval. Intervent
Treatment - Drugs
For Intervention Group: Resveratrol (manufactured by Biovita company), Orally 1gr/day (2 Cap.) for 40 days from the beginning of the menstruation cycle till oocyte retrieval.
For Control Group: Placebo of Resveratrol, Orally 2 Cap. for 40 days from the beginning of the menstruation cycle till oocyte retrieval.

Sponsors

Vice chancellor for research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Infertility with documented PCOS based on Rotterdam criteria; 18-40 Y/O; If have male factor; it must be mild to moderate form, not non-obstructive azospermia; If have other female factor; only cervical & tubal factors are acceptable; Candidate for IVF Cycle; No insulin taking history; Not eating red grapes, pistachio, peanut and berries recently. Exclusion Criteria: Diseases due to obesity with unknown cause (Hypothyroidism, Coshing Syndrome); . FSH>10 at third day of the cycle; Severe endometriosis (Stage III or IV); Thyroid diseases; Congenital Adrenal Hyperplasia; Hyperprolactinemia; Ovarian Tumors; Taking Steroids, OCP and other drugs that affect ovarian function, insulin sensitivity or lipid metabolism in past 3 months (except routin PCOS therapy); SLE (Systemic Lupus Erythematosus) & autoimmune diseases; Systemic diseases like Metabolic Syndrome, Hyperlipidemias & cardiovascular diseases; Severe male factor like non-Obstructive Azospermia (sperm concentration < 5 mill/m); Patients who use vitrification method to avoid OHSS; Having alergy to some fruits like red grapes, pistachio and red berry; Insulin taking history

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
ATF4 Expression. Timepoint: After follicle retrieval (Approximately 40 days after treatment). Method of measurement: Real-time relative quantification.;ATF6 Expression. Timepoint: After follicle retrieval (Approximately 40 days after treatment). Method of measurement: Real-time relative quantification.;CHOP Expression. Timepoint: After follicle retrieval (Approximately 40 days after treatment). Method of measurement: Real-time relative quantification.;GRP78 Expression. Timepoint: After follicle retrieval (Approximately 40 days after treatment). Method of measurement: Real-time relative quantification.;XBP1 Expression. Timepoint: After follicle retrieval (Approximately 40 days after treatment). Method of measurement: Real-time relative quantification.;Inflammatory factors(IL-6, IL-18, IL-1beta, TNF-alpha, CRP). Timepoint: Before & After Intervention. Method of measurement: By ELISA Method.;Insulin Resistance factors( glucose, insulin, homocystein, QUICKI, HOMA-IR). Timepoint: Before & After Intervention. Method of measurement: By Espectrophotometry Method.;Biochemical Factors( FBS, cholestrole, Trigliseride, HDL, LDL). Timepoint: Before & After Intervention. Method of measurement: By Photometry Method.;ROS (Reactive Oxygen Species: PC & MD). Timepoint: After follicle retrieval (Approximately 40 days after treatment) , Before & After Intervention. Method of measurement: By Espectrophotometry Method.;NF-?B Expression. Timepoint: Before & After Intervention. Method of measurement: Real-time relative quantification.;TAC (Total Antioxidant Capacity). Timepoint: After follicle retrieval (Approximately 40 days after treatment) , Before & After Intervention. Method of measurement: By Espectrophotometry Method.;Number of retrieved Oocytes. Timepoint: After Intervention. Method of measurement: Count Under Microscope.;Number of retrieved Mature Oocytes (MII). Timepoint: After Intervention. Method of measurement: Count Under Microscope.;Quality of Retrieved Oocytes. Timepoint: A

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamaneh Brenjian

Tehran University of Medical sciences

sbrenjian@razi.tums.ac.ir smbrenjian@yahoo.com+98 21 2200 5217

Outcome results

None listed

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