Tanshinone in Polycystic Ovary Syndrome
Mots clés
Abstrait
Rendez-vous
Dernière vérification: | 08/31/2013 |
Première soumission: | 10/05/2011 |
Inscription estimée soumise: | 10/11/2011 |
Première publication: | 10/13/2011 |
Dernière mise à jour soumise: | 09/02/2013 |
Dernière mise à jour publiée: | 09/03/2013 |
Date de début réelle de l'étude: | 09/30/2011 |
Date d'achèvement primaire estimée: | 11/30/2013 |
Date estimée d'achèvement de l'étude: | 06/30/2014 |
Condition ou maladie
Intervention / traitement
Drug: tanshinone
Drug: tanshinone placebo
Phase
Groupes d'armes
Bras | Intervention / traitement |
---|---|
Active Comparator: tanshinone tanshinone 1.0g / time, 3 times / day orally, continuous treatment for 12 weeks. | Drug: tanshinone tanshinone 1.0g / time, 3 times / day orally, continuous treatment for 12 weeks. |
Placebo Comparator: tanshinone placebo placebo 1.0g / time, 3 times / day orally, continuous treatment for 12 weeks. | Drug: tanshinone placebo placebo 1.0g / time, 3 times / day orally, continuous treatment for 12 weeks. |
Critère d'éligibilité
Âges éligibles aux études | 18 Years À 18 Years |
Sexes éligibles à l'étude | Female |
Accepte les bénévoles en santé | Oui |
Critères | Inclusion Criteria: - Presence of PCOS diagnosed based on the Androgen Excess Society criteria. All subjects must have hyperandrogenism (hirsutism and/or hyperandrogenemia), ovarian dysfunction (oligoanovulation and/or polycystic ovaries), and exclusion of other androgen excess related disorders. Oligomenorrhea is defined as an intermenstrual interval >35 days or <8 menstrual bleedings in the past year. Amenorrhea is defined as an intermenstrual interval >90 days. Clinical hyperandrogenism is defined as a Ferriman-Gallwey (FG) score ≥5 - Age of women from 18 to 35 years; - No desire of children within 6 month and use condoms for contraception. Exclusion Criteria: - Use of hormonal drugs or other medications, which can affect the results of the study especially Chinese herbal prescriptions in the past 12 weeks; - Patients with other androgen excess endocrine disorders including 21-hydroxylase deficiency, hyperprolactinemia, Cushing syndrome, severe insulin resistance, thyroid dysfunction; - Patients with history of sever cardiac , pulmonary, hepatic, renal, neurologic disease or mental illness; - Pregnancy or lactation. |
Résultat
Mesures des résultats primaires
1. basal testosterone [3 months]
Mesures des résultats secondaires
1. Ovarian androgen biosynthesis [3 months]
2. Whole body insulin action [3 months]
3. Oral glucose tolerance test (OGTT) [3 months]
4. Reproductive hormones [3 months]
5. Fasting gluco-lipid metabolic profiles [3 months]
6. quality of life [3 months]
7. Weight, waist/hip circumference, blood pressure, F-G score and acne before and after treatment [3 months]
8. Adverse events [3 months]