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Efficacy of Bariatric Surgery in the Treatment of Obese Women with Polycystic Ovary Syndrome: A Prospective Clinical Trial

Efficacy of Bariatric Surgery in the Treatment of Obese Women with Polycystic Ovary Syndrome: A Prospective Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013169
Enrollment
Unknown
Registered
2017-10-30
Start date
2017-11-09
Completion date
Unknown
Last updated
2017-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome

Interventions

medication group:medication
bariatric surgery group:bariatric surgery

Sponsors

Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Reproductive women over 18 years old; 2. BMI greater than 27.5 kg/m2; 3. Diagnosed with PCOS (according to The Rotterdam definition,a consensus workshop sponsored by ESHRE/ASRM in Rotterdam in 2003); 4. Able to understand and sign informed consent.;Inclusion criteria: 1. Reproductive women over 18 years old; 2. BMI greater than 27.5 kg/m2; 3. Diagnosed with PCOS (according to The Rotterdam definition,a consensus workshop sponsored by ESHRE/ASRM in Rotterdam in 2003); 4. Able to understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Women with hysterectomy; 2. Patients diagnosed with congenital adrenal hyperplasia, Cushing's syndrome, androgen secreting tumors within five years; 3. Pregnant or lactating mothers; 4. Thrombosis related history or risk factors:deep vein thrombosis,pulmonary embolism,myocardial infarction (angina), valvular heart disease,atrial fibrillation,cerebrovascular accident (TIA); 5. Abnormal liver function caused by viral hepatitisl; 6. A history of liver malignancy or adenoma, a history of genital or breast malignancies; 7. Severe or frequent migraine attacks; 8. Renal insufficiency; 9. Other cases that may affect the efficacy of the drug, or the drugs may compromise the health of the patients.;Exclusion criteria: 1. Women with hysterectomy; 2. Patients diagnosed with congenital adrenal hyperplasia, Cushing's syndrome, androgen secreting tumors within five years; 3. Pregnant or lactating mothers; 4. Thrombosis related history or risk factors:deep vein thrombosis,pulmonary embolism,myocardial infarction (angina), valvular heart disease,atrial fibrillation,cerebrovascular accident (TIA); 5. Abnormal liver function caused by viral hepatitisl; 6. A history of liver malignancy or adenoma, a history of genital or breast malignancies; 7. Severe or frequent migraine attacks; 8. Renal insufficiency; 9. Other cases that may affect the efficacy of the drug, or the drugs may compromise the health of the patients.

Design outcomes

Primary

MeasureTime frame
Ovulation;Menstrual cycle;Ovary structure;Sex hormone levels;body mass index;Waist/hip;blood pressure;serum glucose;glycosylated hemoglobin;serum insulin;serum C-peptide;;Ovulation;Menstrual cycle;Ovary structure;Sex hormone levels;body mass index;Waist/hip;blood pressure;serum glucose;glycosylated hemoglobin;serum insulin;serum C-peptide;

Countries

China

Contacts

Public ContactYin jun;Yin jun ;

Shanghai Jiao Tong University Affiliated Sixth People's Hospital ;Shanghai Jiao Tong University Affiliated Sixth People's Hospital

yinjun@sjtu.edu.cn;yinjun@sjtu.edu.cn+86 18930174165;+86 18930174165

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026