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Clinical Trials/NCT01782911
NCT01782911CompletedNot Applicable

Effect of Resveratrol on Metabolic Parameters and Oocyte Quality in PCOS Patients Undergoing IVF Treatment.

IVI Madrid1 site in 1 country10 target enrollmentStarted: February 1, 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
10
Locations
1
Primary Endpoint
Effect of resveratrol on oocyte quality

Study Overview

Brief Summary

Polycystic ovary syndrome (PCOS) is characterized by enlarged ovaries, menstrual irregularity and hyperandrogenism and is the most common cause of oligoovulatory infertility. Insulin resistance with resulting hyperinsulinemia is also common among women with PCOS, along with increased risk for dyslipidemia, hypertension, diabetes and related cardiovascular consequences. Resveratrol is a natural polyphenol with anti-carcinogenic, anti-proliferative and pro-apoptotic properties, that has been shown to decrease proliferation and steroidogenesis in theca cells, emerging as a potential therapeutic agent in PCOS patients. However, little is known about its potential beneficial effect on oocyte quality as well as other reproductive outcomes, such as implantation an pregnancy rates. The present study evaluates effects of resveratrol on selected biochemical parameters and reproductive outcome among patients with PCOS who undergo in vitro fertilization (IVF).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Women aged from 18 to 40 years old.
  • •PCOS diagnosis (according to Rotterdam criteria).
  • •Mild or moderate male factor, tubal factor or unknown infertility.

Exclusion Criteria

  • •Follicle stimulation hormone (third of day of menstruation) > 10 milli international units/L.
  • •Endometriosis (III o IV).
  • •Congenital adrenal hyperplasia.
  • •Cushing syndrome.
  • •Hyperprolactinemia.
  • •Thyroid disease.
  • •Androgenic hormone secretor tumors.
  • •Patients included in this trial did not take either oral contraceptives, steroids or other medications that could modify the ovarian function, insulin sensitivity or lipid metabolism 3 months before the onset of the trial.
  • •Severe male factor (sperm concentration < 5 mill/ml).
  • •Patients undergoing oocyte vitrification to avoid hyperstimulation syndrome will be excluded.

Arms & Interventions

Control

Placebo Comparator

Patients will be given pills lacking medication from the onset of menses until the ovum pick-up.

Intervention: Placebo pills (Dietary Supplement)

Resveratrol

Experimental

Patients will be given 2 g of resveratrol a day from the onset of menses until ovarian pick-up.

Intervention: Resveratrol (Dietary Supplement)

Outcomes

Primary Outcomes

Effect of resveratrol on oocyte quality

Time Frame: 40 days

Secondary Outcomes

  • Effect of resveratrol on testosterone levels.(40 days)
  • Effects of resveratrol on the fertilization rate.(40 days)
  • Effects of resveratrol on the pregnancy rate.(40 days)
  • Effects of resveratrol on inflammatory markers(40 days)

Investigators

Sponsor
IVI Madrid
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Juan A Garcia-Velasco

Medical Doctor

IVI Madrid

Study Sites (1)

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