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Clinical Trials/NCT03151005
NCT03151005
Completed
Phase 4

Randomized Clinical Trial to Evaluate The Effect of Metformin-GLP-1 Receptor Agonist Versus Oral Contraceptive (OC) Therapy on Reproductive Disorders and Cardiovascular Risks in Overweight Polycystic Ovarian Syndrome (PCOS) Patients

Xinqiao Hospital of Chongqing1 site in 1 country70 target enrollmentJuly 1, 2017

Overview

Phase
Phase 4
Intervention
Metformin-GLP-1 Receptor Agonist
Conditions
Polycystic Ovary Syndrome (PCOS)
Sponsor
Xinqiao Hospital of Chongqing
Enrollment
70
Locations
1
Primary Endpoint
Assessment of Reproductive Functions
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Polycystic ovary syndrome (PCOS) is a health problem that affects one in 10 women of childbearing age, which is usually characterized by hormonal imbalance and metabolism problems such as hyperandrogenism and obesity. Diane 35 pills are classified as oral contraceptives, which effectively reduces circulating androgens and are treatment for hyperandrogenism caused androgenic skin symptoms and irregular menstrual cycles. GLP-1 Receptor Agonist(e.g. exenatide, liraglutide) have the effects of lowering blood sugar and weight control by inhibiting of gastric emptying and reducing food intake. This study aims to evaluate the effect of metformin-GLP-1 Receptor agonist combination versus metformin-Diane-35 combination treatment on lipid metabolism and cardiovascular risks in overweight polycystic ovarian syndrome (PCOS) patients.

Detailed Description

Groups: Experimental treatment: Metformin-GLP-1 Receptor Agonist Therapy. Regular treatment: Metformin-Oral Contraceptive(OC) Therapy. Time Point: Initial treatment; Post-treatment (4w); Post-treatment (8w); Post-treatment (12w); Assess reproductive functions and cardiovascular risk factors.

Registry
clinicaltrials.gov
Start Date
July 1, 2017
End Date
April 23, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Xinqiao Hospital of Chongqing
Responsible Party
Principal Investigator
Principal Investigator

Long Min,MD

Deputy Chief Physician, Associated professor

Xinqiao Hospital of Chongqing

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of PCOS according to the Rotterdam criteria based on the presence of two of three criteria: oligomenorrhoea, clinical or biochemical hyperandrogenism and polycystic ovaries on ultrasound after exclusion of other endocrine causes of hyperandrogenism.
  • Participants had no concurrent illness and were not on any prescription or over-the-counter medication that was likely to affect insulin sensitivity or lipids for the preceding 12 weeks.
  • Participants were advised not to change physical activity or dietary habits during the study period. All subjects were overweight/obese \[body mass index (BMI) \>=24 kg/m2 or waistline\>=85cm \].
  • All subjects had normal thyroid-stimulating hormone and prolactin levels.

Exclusion Criteria

  • smoking, alcohol use, or having taken medication within 2 months of the study that is known to affect reproductive or metabolic functions.
  • age below 18 yr or over 50 yr.
  • postmenopausal.
  • uncontrolled hypertension (blood pressure \>=160/100 mm Hg).
  • preexisting OPs or GLP-1 agonists supplementation
  • alcohol intake greater than 20 g/d, or pregnancy.
  • signs of liver or renal failure or active liver disease (ALT \> 2.5× the upper limit of normal values).
  • PLT\<60\*10\^9/L,Hb\<100g/L, smoking, alcohol use.
  • The patient that cannot complete the intervention or have other conditions that is not appropriate to enter the group, such as patients who are taking glucocorticoid steroids or malignant tumor treatment, etc.

Arms & Interventions

Metformin-GLP-1 Receptor Agonist

Metformin-GLP-1 Receptor Agonist Therapy: metformin 0.5 g/time by mouth, 3 times per day, with 5 ug exenatide subcutaneous injection twice per day, for 4 weeks, then change to 10ug exenatide subcutaneous injection twice per day for 8 weeks; or metformin 0.5 g/time by mouth, 3 times per day, with 0.6mg liraglutide subcutaneous injection once per day, for 1 weeks, then change to 1.2-1.8 mg liraglutide subcutaneous injection according to patient's blood glucose condition, twice per day for 8 weeks.

Intervention: Metformin-GLP-1 Receptor Agonist

Metformin-Oral Contraceptive(OC)

Metformin-Oral Contraceptive(OC) Therapy: metformin 0.5 g/ time by mouth, 3 times per day, with Diane 35(OC) 1 piece per day by mouth, for 12 weeks.

Intervention: Metformin-Oral Contraceptive(OC)

Outcomes

Primary Outcomes

Assessment of Reproductive Functions

Time Frame: 12 weeks

Concentration of LH was measured in mIU/ml.

Secondary Outcomes

  • Basic Vital Signs(12 weeks)
  • Assessment of Liver Function(12 weeks)
  • Assessment of Blood Pressure(12 weeks)
  • Assessment of Reproductive Function(12 weeks)

Study Sites (1)

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