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Interest of Myo-inositol Supplementation in Women With Polycystic Ovarian Syndrome — MYOPK  

Polycystic Ovary Syndrome Clinical Trial

Official title:
Interest of Myo-inositol Supplementation in Women With Polycystic Ovarian Syndrome During Induction of Ovulation With Clomiphene Citrate

Clinical Trial Summary

The main objective will be to check if MyoInositol (MYO) reduces the total resistance rate to Clomiphene Citrate (CC). For this, our study will be controlled, randomized and double blinded. It will include patients with PCOS (polycystic ovary syndrome, defined by the Rotterdam criteria) who wish to become pregnant and are eligible to simple ovulation induction by CC. Half of them will receive MYO + levomefolic acid (5-MTHF) in addition to the CC, while the other half will receive a placebo containing only 5-MTHF in addition to the CC. The MYO supplementation will be initiated at least one month before taking CC and will be continued throughout this treatment until pregnancy or before switching to another type of treatment for ovulation induction if no pregnancy is obtained after 6 ovulatory cycles.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03059173
Study type Interventional
Source University Hospital, Lille
Contact Goeffrey ROBIN, MD
Phone 320446252
Email goeffrey.robin@chru-lille.fr
Status Recruiting
Phase Phase 3
Start date September 12, 2023
Completion date December 2027
View Details
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