Metformin Suspension and Insulin Sensitivity
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Metformin cloridrate
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Insulin sensitivity, Insulin-sensitizing drug, Metformin, PCOS, Treatment
Eligibility Criteria
Inclusion Criteria:
- Polycystic ovary syndrome (using NIH criteria).
Exclusion Criteria:
- Age <20 or >30 years;
- BMI higher than 25 and lower than 18;
- Neoplastic, metabolic, hepatic, and cardiovascular disorders or other concurrent medical illnesses;
- Hypothyroidism, hyperprolactinemia, Cushing's syndrome, and non-classical congenital adrenal hyperplasia;
- Current or previous use of oral contraceptives, glucocorticoids, antiandrogens, ovulation induction agents, antidiabetic and anti-obesity drugs or other hormonal drugs;
- Intention to start a diet or a specific program of physical activity.
Sites / Locations
- "Pugliese" Hospital
Outcomes
Primary Outcome Measures
Insulin sensitivity by euglycemic hyperinsulinemic clamp
Secondary Outcome Measures
Clinical, hormonal, and metabolic assessments
Full Information
NCT ID
NCT00437333
First Posted
February 20, 2007
Last Updated
February 20, 2007
Sponsor
University Magna Graecia
1. Study Identification
Unique Protocol Identification Number
NCT00437333
Brief Title
Metformin Suspension and Insulin Sensitivity
Official Title
Insulin Sensitivity After Metformin Suspension in Normal-Weight Women With Polycystic Ovary Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
February 2007
Overall Recruitment Status
Completed
Study Start Date
December 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University Magna Graecia
4. Oversight
5. Study Description
Brief Summary
Metformin is an insulin sensitizing drug routinely used for the treatment of anovulatory patients with polycystic ovary syndrome (PCOS). To date, the metabolic effects of the long-term metformin administration are know but no data are available on the effects after its suspension.
The purpose of this study is to evaluate the effects of metformin suspension on insulin sensitivity in PCOS patients.
Detailed Description
Thirty young normal-weight anovulatory PCOS women will be enrolled. The diagnosis of PCOS will be based on the presence of clinical [Ferriman-Gallwey score ≥ 8] or biochemical hyperandrogenism (serum testosterone levels (>2 SD above our reference mean values) and chronic anovulation [serum luteal progesterone (P) below 2 ng/mL)].
Patients will be randomly allocated into two groups (metformin and placebo group) using a computer-software. Fifteen PCOS patients will be treated with metformin at a dosage of 1700 mg daily (one tablet of 850 mg twice daily; metformin group), whereas other 15 PCOS will be treated with placebo tables (one tablet twice daily; placebo group). The duration of the treatment will be 12 months. Patients will be instructed to follow their usual diet and physical activity, and to use barrier contraception throughout the study. The length and the frequency of the menstrual cycles, and the adverse experiences (AEs) will be reported on a daily diary.
Each subject will undergo follow-up visits under (at six and 12 months from treatment starting) and after treatment (at six and 12 months from treatment withdrawal). At each follow-up visit, in all subjects the same operator will perform clinical, hormonal, metabolic, and insulin sensitivity assessments by euglycemic hyperinsulinemic clamp.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
Insulin sensitivity, Insulin-sensitizing drug, Metformin, PCOS, Treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
30 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Metformin cloridrate
Primary Outcome Measure Information:
Title
Insulin sensitivity by euglycemic hyperinsulinemic clamp
Secondary Outcome Measure Information:
Title
Clinical, hormonal, and metabolic assessments
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Polycystic ovary syndrome (using NIH criteria).
Exclusion Criteria:
Age <20 or >30 years;
BMI higher than 25 and lower than 18;
Neoplastic, metabolic, hepatic, and cardiovascular disorders or other concurrent medical illnesses;
Hypothyroidism, hyperprolactinemia, Cushing's syndrome, and non-classical congenital adrenal hyperplasia;
Current or previous use of oral contraceptives, glucocorticoids, antiandrogens, ovulation induction agents, antidiabetic and anti-obesity drugs or other hormonal drugs;
Intention to start a diet or a specific program of physical activity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefano Palomba, MD
Organizational Affiliation
Department of Obstetrics and Gynecology, University "Magna Graecia" of Catanzaro
Official's Role
Principal Investigator
Facility Information:
Facility Name
"Pugliese" Hospital
City
Catanzaro
ZIP/Postal Code
88100
Country
Italy
12. IPD Sharing Statement
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Metformin Suspension and Insulin Sensitivity
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