Polycystic ovary syndrome
Conditions
Interventions
Experimental group:Companion lifestyle intervention combined with medication
Sponsors
Shenzhen Hospital of Southern Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: (1) Diagnosis of PCOS (according to the Rotterdam criteria 2003) and exclude other diseases that may cause hyperandrogen and abnormal ovulation. (2) Obesity (BMI>= 28 kg/m^2) or overweight (BMI=24kg/m^2 and BMI < 28 kg/m^2) (3) Female aged 22-40 years (4) Voluntarily sign informed consent
Exclusion criteria
Exclusion criteria: (1) Pregnant or lactating women; (2) Hyperandrogenemia caused by other disease; (3) Combined with other endocrine diseases, such as diabetes, pituitary-adrenal diseases, clinical thyroid diseases, acromegaly, prolactinoma, androgen secreting tumors, etc; (4) Previous or current chronic diseases that may interfere with the study; (5) Severe acute illness that may interfere with the study; (6) Have taken hormone drugs in recent 3 months; (7) History of severe mental illness, drug use, and recent major life events; (8) Difficult to cooperate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Follicles;menstruation; | — |
Secondary
| Measure | Time frame |
|---|---|
| BMI;follicle-stimulating hormone;luteinizing hormone;total testosterone;short form 36 questionnaire; | — |
Countries
China
Contacts
Public ContactXu Lingling
Shenzhen Hospital of Southern Medical University
Outcome results
None listed