Polycystic Ovary Syndrome and Liraglutide
Study Details
Study Description
Brief Summary
The purpose of this study was to determine whether liraglutide is more effective than metformin in the treatment of obese women with newly diagnosed polycystic ovary syndrome (PCOS). We anticipated greater changes in body weight in patients treated with liraglutide than in those treated with metformin.
Condition or Disease | Intervention/Treatment | Phase |
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Phase 4 |
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Active Comparator: metformin In the MET group metformin was initiated at a dose of 500 mg once per day and increased by 500 mg every 3 days up to 1000 mg BID per os. |
Drug: metformin
Other Names:
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Experimental: liraglutide In the LIRA group liraglutide was initiated at a dose of 0.6 mg injected sc once per day and increased to 1.2 mg/day after 1 week. |
Drug: liraglutide
Other Names:
|
Outcome Measures
Primary Outcome Measures
- The main outcome was change in body weight. [Patient's body weight was mesured at the base point and every four weeks during 12 weeks of clinical trial.]
Secondary Outcome Measures
- The secondary outcome was change in body mass index (BMI) [Patient's body weight were measured at the base point and every four weeks during the 12 weeks of clinical trial. Patient's height was measured at the basepoint.]
Patient's BMI was defined as the patient's body mass in kilograms divided by the square of their height in meters.
- The secondary outcome was change in waist circumference. [Patient's waist circumference was measured at the basepoint and every four weeks during 12 weeks of clinical trial.]
Patient's waist circumference was measured in centimeters.
Other Outcome Measures
- The other outcomes was changes changes in fasting concentrations of glucose. [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial.]
Patient's blood was drawn between 8 and 9 a.m. Concentrations of fasting glucose was measured in mmol/L.
- Other outcome was change in fasting concentration of insulin. [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial.]
Patient's blood was drawn between 8 and 9 a.m. Fasting concentrations of insulin was measured in mU/L.
- Other outcome was change in blood concentrations of LH (luteinizing hormone). [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial]
Patient's blood was drawn between 8 and 9 a.m. Comncetration of LH was measured in U/L.
- Other outcome was change in blood concentrations of FSH (follicle-stimulating hormone). [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial]
Patient's blood was drawn between 8 and 9 a.m. Blood concentrations of FSH was measured in U/L.
- Other outcome was change in blood concentration of testosterone. [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial.]
Patient's blood was drawn between 8 and 9 a.m. Blood concentration was measured in nmol/L.
- Otehr outcome was change in blood concentration in androstenedione. [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial]
Patient's blood was drawn between 8 and 9 a.m. Blood concentrations of androstenedione was measured in nmol/L.
- Other outcome was change in blood concentrations of SHBG (sex hormone-binding globulin). [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial]
Patient's blood was drawn between 8 and 9 a.m. Blood concentrations of SHBG was measured in nmol/L.
- Other outcome was change in blood concentration of DHEAS (dehydroepiandrosterone sulfate) [Patient's fasting blood was drawn at the basepoint and every four weeks during the 12 weeks of clinical trial.]
Patient's blood was drawn between 8 and 9 a.m. Blood concentrations of DHEAS was measured in micromol/L.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
18 years old to menopause
-
polycystic ovary syndrome (NICHD criteria)
-
BMI of 30 kg/m² or higher
Exclusion Criteria:
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type 1 or type 2 diabetes mellitus
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history of carcinoma
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Cushing's syndrome or congenital (non-classic) adrenal hyperplasia
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personal or family history of MEN 2
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significant cardiovascular, kidney or hepatic disease
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the use of medications known or suspected to affect reproductive or metabolic functions
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the use of statins, within 90 days prior to study entry
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | University Medical Center Ljubljana | Ljubljana | Slovenia | 1000 |
Sponsors and Collaborators
- University Medical Centre Ljubljana
Investigators
- Principal Investigator: Andrej Janez, MD, PhD, University Medical Centre Ljubljana
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 20120047