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Efficacy of Empagliflozin in overweight and obese women with polycystic ovary syndrome: A single-center prospective randomized controlled trial

Efficacy of Empagliflozin on the improvement of metabolism and hormones in overweight and obese women with polycystic ovary syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090908
Enrollment
Unknown
Registered
2024-10-15
Start date
2024-04-05
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Polycystic ovary syndrome

Interventions

The group of Empagliflozin:Empagliflozin
The group of Metformin:Metformin

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: ? Age:18-40 years old; ? BMI:24.0-38.0 kg/m2; ? Not combined with other serious chronic diseases; ? Normal liver function, renal function and electrocardiogram examination; ? Meeting the diagnostic criteria of polycystic ovary syndrome and excludes other diseases such as congenital adrenal cortical hyperplasia, Cushing's syndrome, and androgen secreting tumors. ? Fully understanding the trial content, voluntarily participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? With diabetes (type 1 or type 2) ? With chronic diseases of heart, liver, or kidney; Individuals with drug allergy, allergic diseases or allergic constitution; Smokers and alcoholics; ? Concomitant Cushing's syndrome, congenital adrenal hyperplasia, benign and malignant tumors of various systems, liver and kidney dysfunction, organic heart disease, rheumatoid arthritis, systemic lupus erythematosus, polycystic kidney disease, psychiatric disorders, HIV/tuberculosis/HCV and other chronic diseases; ? Having a history of using glucocorticoids, estrogen, progesterone or insulin within 3 months prior to enrollment; ? Being unable to cooperate with follow-up due to personal reasons; ? Being in gestation or preparing for pregnancy; ?In addition, it also includes: 1) patients who are participating in other clinical trials within one month before the trial; 2) Researchers believe that other reasons are not suitable for clinical trial participants

Design outcomes

Primary

MeasureTime frame
weight;body mass index;sex hormone;

Secondary

MeasureTime frame
glycated hemoglobin A 1c (HbA1c);triglyceride(TG);total cholesterol(TC);high density lipoprotein cholesterol(HDL-C);Apolipoprotein B (apo B);Oral Glucose Tolerance Test (OGTT);Oral Glucose Insulin Release Test(OGIRT);

Countries

China

Contacts

Public ContactDongfang Liu

The Second Affiliated Hospital of Chongqing Medical University

ldf023023@qq.com+86 186 2340 7751

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 5, 2026