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Metformin Suspension and Insulin Sensitivity

Insulin Sensitivity After Metformin Suspension in Normal-Weight Women With Polycystic Ovary Syndrome

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00437333
Enrollment
30
Registered
2007-02-21
Start date
2003-12-31
Completion date
2006-04-30
Last updated
2007-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome

Keywords

Insulin sensitivity, Insulin-sensitizing drug, Metformin, PCOS, Treatment

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.

Interventions

DRUGMetformin cloridrate

Sponsors

University Magna Graecia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 30 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Insulin sensitivity by euglycemic hyperinsulinemic clamp

Secondary

MeasureTime frame
Clinical, hormonal, and metabolic assessments

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026