Evaluation of Metionac for the Modulation of Metabolic and Endocrine Parameters in Patients With PCOS.
Polycystic Ovary Syndrome
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome
Eligibility Criteria
Inclusion Criteria:
Women newly diagnosed with PCOS with at least 2 of the following symptoms:
- Oligo/Anovulation < 21 or > 35 days > 90 days (any cycle) < 8 periods / year
- Hyperandrogenism (clinical symptoms or laboratory results)
Polycystic ovary morphology (NHMRC guideline): In any ovary:
20 follicles* and/or ovarian volume greater than or equal to 10ml and no corpus luteum, cysts or dominant follicles
*number of follicles per ovary measuring 2-9 mm
- > 18 years old
- Overweight defined as BMI>25
- Normal prolactin levels
- Women with altered coagulation factors or a personal history of thromboembolism for whom OAC is contraindicated (they will be included in the control group without randomization)
- Written inform consent
Exclusion Criteria:
- Diabetic women
- Adrenal enzyme deficiency and/or other endocrine disease
- Pregnant or lactating women.
- Women under treatment with SNRIs (serotonin reuptake inhibitors)
- Other serious illness
Sites / Locations
- Hospital Quironsalud San José
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Experimental
Other
Oral Contraceptive
Oral Contraceptive + Food supplement Metionac
Food supplement MetioNac
Drospirenone 4 mg once a day for 6 months
Drospirenone 4 mg once a day and Metionac twice daily (200 mg S-adenosylmethionine, 100 mg N-acetylcisteine, 75 mg alpha lipoid acid and 0,65 Vitamin B6) for 6 months
Metionac twice daily (200 mg S-adenosylmethionine, 100 mg N-acetylcisteine, 75 mg alpha lipoid acid and 0,65 Vitamin B6) for 6 months