Effects of Pioglitazone Combined With Metformin on Gonadal and Metabolic Profiles in Chinese Nonobese PCOS Patients.
1 other identifier
interventional
60
1 country
1
Brief Summary
To study the effects of pioglitazone combined with metformin and metformin on gonadal and metabolic profiles in PCOS patients with BMI \< 24 in China. 60 cases of nonobese PCOS patients were collected from Shengjing hospital. The intervention period was 3 months after intervention with met or met + ph. To evaluate the improvement of met or met + ph in the treatment of hyperandremia, glucose metabolism, BMI, waist circumference, menstruation, hairiness and acne in PCOS patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4
Started Jan 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2022
CompletedFirst Submitted
Initial submission to the registry
April 13, 2022
CompletedFirst Posted
Study publicly available on registry
August 29, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
March 20, 2023
CompletedAugust 29, 2022
August 1, 2022
1 year
April 13, 2022
August 25, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Changes in sex hormone binding globulin (SHBG)
Changes in sex hormone binding globulin (SHBG)
12 weeks
Secondary Outcomes (13)
Changes in free testosterone (FT)
12 weeks
Changes in Luteinizing Hormone (LH)
12 weeks
Changes in follicle stimulating hormone (FSH)
12 weeks
Changes in total testosterone (TT)
12 weeks
Changes in dehydroepiandrosterone sulfate (DHEAS)
12 weeks
- +8 more secondary outcomes
Study Arms (2)
Use Metformin for 3 months to treat PCOS
EXPERIMENTALActive Comparator: Metformin (BMI\<24) Subjects: PCOS patients whoseBMI\<24 Drug: Glucophage Generic name: Metformin Dosage form: 500mg Dosage: 1500-2000mg/day Frequency: 500mg three times a day/1000mg twice a day Duration: 3 months
Use Pioglitazone Hydrochloride And Metformin Hydrochloride Tablets for 3 months to treat PCOS
EXPERIMENTALActive Comparator: Pioglitazone Hydrochloride And Metformin Hydrochloride Tablets (BMI\<24) Subjects: PCOS patients whoseBMI\<24 Drug: Pioglitazone Hydrochloride And Metformin Hydrochloride Tablets Generic name: Pioglitazone Hydrochloride And Metformin Hydrochloride Tablets Dosage form: 15mg/500mg Dosage: 2 tablets/day Frequency: one tablet twice a day Duration: 3 months
Interventions
Use Pioglitazone Hydrochloride And Metformin Hydrochloride Tablets for 3 months to treat PCOS
Eligibility Criteria
You may qualify if:
- Females 18 years to 40 years of age Diagnosed as PCOS by the 2003 Rotterdam criteria
- BMI\<24 kg/m2
- No pregnant plan in recent 6 months
- Written consent for participation in the study
You may not qualify if:
- type 1 or type 2 diabetes mellitus
- Subjects have other endocrine diseases, such as adrenal hyperplasias or tumor, androgen-secreting tumors, Cushing's syndrome, thyroid diseases, and hyperprolactinemia
- Diagnosed with or have a family history of medullary thyroid carcinoma (MTC) or Multiple Endocrine Neoplasia syndrome type 2 (MEN 2)
- Serious systemic disease or malignant tumor
- History of pancreatitis (chronic, acute or recurrent)
- Body weight change ≥10% at 3 months before treatment
- Used oral contraceptives or sex hormone drugs in the past 1 month
- Used oral glucocorticoids in the past 1 month
- Substance (alcohol or drug) abuse or dependence within 3 months
- Heavy smokers (smokers who smoke 20 or more cigarettes a day) or heavy drinkers (\>10g/d)
- Subjects have a severe systemic disease, such as cardiovascular system, Renal impairment (eGFR\<60ml/min/1.73m2)
- Increase of transaminases up to \< 2.5 times of upper limit of normal value
- Have a history of thromboembolic disease or thrombotic tendency
- Subjects in pregnant or lactating or within 1 year after delivery
- Subjects have an allergic history to the drugs used in the study
- +3 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Bing Helead
Study Sites (1)
Shengjing Hospital of China Medical University
Shenyang, Liaoning, 110004, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 13, 2022
First Posted
August 29, 2022
Study Start
January 1, 2022
Primary Completion
January 1, 2023
Study Completion
March 20, 2023
Last Updated
August 29, 2022
Record last verified: 2022-08