About this trial
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.
Eligibility criteria
Qualifiers
Wishing pregnancy,
Having PCOS defined by the Rotterdam criteria: high antral follicle count (AFC) (> 19 per ovary) and/or a disorder of the cycle and/or hyperandrogenism (at least two of the three criteria),
Having never been treated with CC (or previous treatment with CC interrupted for > 3 months).
Having received complete information and having signed consent.
Disqualifiers
Intolerance to CC in previous treatment,
BMI > 35,
Other associated cause of oligoanovulation requiring specific treatment (eg., Hyperprolactinemia or functional hypothalamic anovulation),
Ongoing pregnancy at the time of CC initiation,
Trial design
Treatments tested in this trial
- Myo-Inositol + Levomefolic acid
- Clomiphene Citrate
- placebo
Treatment groups
Sponsors and collaborators
University Hospital, Lille
Lead sponsor
Ministry of Health, France
Collaborator
Laboratoires Besins International
Collaborator