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The Effect of GLP-1 Agonists Versus OCs on Reproductive Disorders and Cardiovascular Risks in Overweight PCOS

Phase 4
Completed
Conditions
Obesity
Overweight
Polycystic Ovary Syndrome (PCOS)
Interventions
Drug: Metformin-GLP-1 Receptor Agonist
Drug: Metformin-Oral Contraceptive(OC)
Registration Number
NCT03151005
Lead Sponsor
Xinqiao Hospital of Chongqing
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
70
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Metformin-GLP-1 Receptor AgonistMetformin-GLP-1 Receptor AgonistMetformin-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.
Metformin-Oral Contraceptive(OC)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.
Primary Outcome Measures
NameTimeMethod
Assessment of Reproductive Functions12 weeks

Concentration of LH was measured in mIU/ml.

Secondary Outcome Measures
NameTimeMethod
Basic Vital Signs12 weeks

Weight and height will be combined to report BMI in kg/m\^2.

Assessment of Liver Function12 weeks

Alanine transaminase was measured in IU/L.

Assessment of Blood Pressure12 weeks

Systolic blood pressure was measured in mmHg.

Assessment of Reproductive Function12 weeks

Changes in testosterone levels were measured

Trial Locations

Locations (1)

The Second Affiliated Hospital, Third Military Medical University

🇨🇳

Chongqing, Chongqing, China

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