About this trial
Based on available evidence and given the potential beneficial effects of resveratrol in folliculogenesis and in oocyte development, the investigators designed a randomized, controlled, double-blind, single-center trial, whose objective will be the comparison of biological and clinical outcomes of resveratrol supplement in women undergoing IVF/ICSI cycles for unexplained infertility.
To the knowledge of the investigators, no study has been published on the potential effect of resveratrol on IVF/ICSI outcomes considering couples with this infertility diagnosis, which may be the natural target of this integrative treatment because the process of folliculogenesis and oocyte maturation cannot be routinely investigated. An alteration of these biological mechanisms could be the unrecognized cause of part of the unexplained infertility and treatment with resveratrol could result in significant clinical improvement for the patients enrolled in the study.
In more details, the main objective of this randomized, placebo-controlled, double-blind, single-center trial will be the evaluation of the possible effect of resveratrol in determining a better follicle development in patients with unexplained infertility undergoing controlled ovarian stimulation (COS) for IVF/ICSI.
Infertile female patients with normal ovarian reserve will be treated according to clinical practice and the difference between expected (through AFC) and retrieved oocytes will be assessed in relation to use of resveratrol.
Eligibility criteria
Qualifiers
Female age 18-40 years
Female BMI 18-30 kg/m2
normal menstrual cycles (26-35 days)
duration of infertility at least 18 months
Disqualifiers
≥15 cigarettes per day at least in one of the partners
irregular menstrual cycles
poor ovarian response (on the basis of the "Bologna" Criteria)
inaccessible ovaries
Trial design
Treatments tested in this trial
- Resveratrol-based multivitamin supplement
- Folic acid
- IVF/ICSI
- Follitropin Alfa
- Ganirelix Acetate 0.5 MG/ML [Fyremadel]
- hCG 10.000 IU or triptorelin 0,3 mg, subcutaneously