Metformin and Oral Contraceptives in PCOS
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Metformin
Desorelle
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Polycystic ovary syndrome
Eligibility Criteria
Inclusion Criteria:
- Irregular menses or anovulaty cycles
- High free testosterone > 0.035 nmol/l or hirsutism
- PCO in vaginal US Criteria 1 and 2 OR 2 and 3
Exclusion Criteria:
- Age > 18 years
- Postmenopausal
- Diagnosis diabetes mellitus
- Use of medicine known to affect hormones measured in the project
- Pregnancy or planned pregnancy during study period
- Non-Caucasian
- Previous tromboembolic disease
- Heavy smoker > 35 years and BMI > 35 kg/m2
Sites / Locations
- Odense University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
1
2
3
Arm Description
metformin
desorelle
desorelle + metformin
Outcomes
Primary Outcome Measures
Changes in fasting insulin and area under the curve for insulin (2 hours)
Secondary Outcome Measures
Changes in BMD, BMI, WHR, LH, FSH, total and free testosterone, fasting blood glucose, fasting C-peptide, urine-cortisol secretion, body composition, number of hypoglycaemic cases, AUC for insulin, glucose and C-peptide during OGTT (2 and 5 ho
Changes in cortisol metabolism
Changes in the prevalence of reactive hypoglycemia and areal under the curve for glucose (5 hours)
Full Information
NCT ID
NCT00451568
First Posted
March 22, 2007
Last Updated
April 10, 2015
Sponsor
Odense University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00451568
Brief Title
Metformin and Oral Contraceptives in PCOS
Official Title
Metformin and Oral Contraceptives in PCOS
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
March 2007 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background: PCOS is a common condition with a prevalence of 5-8 % in premenopausal women. More than 50% of PCOS patients are insulin resistant and have a diabetes risk 5-8 times higher than age- and weight-matched controls. Studies using insulin sensitizers in PCOS found increased insulin sensitivity and decreased insulin levels to be followed by decreased androgen levels and improved ovulatory function. No studies however, evaluated the long term effects of insulin sensitizing treatment.
Oral contraceptives normalize menstrual cycles and suppress androgen levels in PCOS, however no long-term studies evaluated the effects of combined treatment with metformin and oral contraceptives in PCOS.
Design: Randomized open study in 3*30 PCOS patients. Patients are randomised to 24 months of treatment with 1: metformin, 2: metformin and oral contraceptives or 3: oral contraceptives.
Primary outcome measures: fasting insulin, AUC insulin. Secundary endpoints: BMI, WHR, LH, FSH, total and free-testosterone, c-peptid, urinary cortisol, AUC for insulin, glucose and c-peptid during OGTT.
Inclusioncriteria:
Irregular menses or anovulaty cycles
High free testosterone > 0,035 nmol/l or hirsutism
PCO in vaginal US Criteria 1 and 2 OR 2 and 3.
Design:
Detailed Description
90 patients are included and randomized to 12 months of treatment with metformin (1000+1000 mg/d) or OCP (150 mg desogestrel 30 microgram ethinylestradiol) or combined treatment (metformin+OCP).
Patients attend a biochemical and physical examination at study inclusion and at 12 months. Patients attend for registration of side effects and compliance after 6 months of study duration. Safety tests are performed at all three visits and include weight, blood pressure, HbA1c, liver enzymes, electrolytes, and white blood cell count. Pregnancy tests are performed by the participants each month. Patients are given general advice on lifestyle intervention. Patients are excluded if they initiated medical treatment with possible hormonal and metabolic effects during the intervention period. Lifestyle intervention is allowed. Laser treatment is offered to patients with moderate or severe facial hirsutism and patients are allowed to shave/wax. The patients accept not applying cosmetic treatment 3-4 days before attending for evaluation at the clinic.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
Polycystic ovary syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
metformin
Arm Title
2
Arm Type
Active Comparator
Arm Description
desorelle
Arm Title
3
Arm Type
Active Comparator
Arm Description
desorelle + metformin
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
500 mg 2 tablets 2 times a day
Intervention Type
Drug
Intervention Name(s)
Desorelle
Intervention Description
1 tablet/day in 21 days
Primary Outcome Measure Information:
Title
Changes in fasting insulin and area under the curve for insulin (2 hours)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Changes in BMD, BMI, WHR, LH, FSH, total and free testosterone, fasting blood glucose, fasting C-peptide, urine-cortisol secretion, body composition, number of hypoglycaemic cases, AUC for insulin, glucose and C-peptide during OGTT (2 and 5 ho
Time Frame
12 months
Title
Changes in cortisol metabolism
Time Frame
12 months
Title
Changes in the prevalence of reactive hypoglycemia and areal under the curve for glucose (5 hours)
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Irregular menses or anovulaty cycles
High free testosterone > 0.035 nmol/l or hirsutism
PCO in vaginal US Criteria 1 and 2 OR 2 and 3
Exclusion Criteria:
Age > 18 years
Postmenopausal
Diagnosis diabetes mellitus
Use of medicine known to affect hormones measured in the project
Pregnancy or planned pregnancy during study period
Non-Caucasian
Previous tromboembolic disease
Heavy smoker > 35 years and BMI > 35 kg/m2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marianne Andersen, MD, PhD
Organizational Affiliation
Odense University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Odense University Hospital
City
Odense
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
27529295
Citation
Glintborg D, Petersen MH, Ravn P, Hermann AP, Andersen M. Comparison of regional fat mass measurement by whole body DXA scans and anthropometric measures to predict insulin resistance in women with polycystic ovary syndrome and controls. Acta Obstet Gynecol Scand. 2016 Nov;95(11):1235-1243. doi: 10.1111/aogs.12964.
Results Reference
derived
PubMed Identifier
27008892
Citation
Mumm H, Altinok ML, Henriksen JE, Ravn P, Glintborg D, Andersen M. Prevalence and possible mechanisms of reactive hypoglycemia in polycystic ovary syndrome. Hum Reprod. 2016 May;31(5):1105-12. doi: 10.1093/humrep/dew046. Epub 2016 Mar 23.
Results Reference
derived
PubMed Identifier
24906976
Citation
Glintborg D, Mumm H, Altinok ML, Richelsen B, Bruun JM, Andersen M. Adiponectin, interleukin-6, monocyte chemoattractant protein-1, and regional fat mass during 12-month randomized treatment with metformin and/or oral contraceptives in polycystic ovary syndrome. J Endocrinol Invest. 2014 Aug;37(8):757-764. doi: 10.1007/s40618-014-0103-8. Epub 2014 Jun 7.
Results Reference
derived
PubMed Identifier
24742124
Citation
Glintborg D, Altinok ML, Mumm H, Hermann AP, Ravn P, Andersen M. Body composition is improved during 12 months' treatment with metformin alone or combined with oral contraceptives compared with treatment with oral contraceptives in polycystic ovary syndrome. J Clin Endocrinol Metab. 2014 Jul;99(7):2584-91. doi: 10.1210/jc.2014-1135. Epub 2014 Apr 17.
Results Reference
derived
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Metformin and Oral Contraceptives in PCOS
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