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| Sponsor: | University of Oulu |
|---|---|
| Collaborators: |
University of Eastern Finland Helsinki University University of Tampere University of Turku |
| Information provided by: | University of Oulu |
| ClinicalTrials.gov Identifier: | NCT00994812 |
Purpose
The purpose of this study is to determine whether metformin may improve pregnancy rates, and decrease miscarriage rates and complications of pregnancy, such as toxemia and gestational diabetes, in women with polycystic ovary syndrome (PCOS).
| Condition | Intervention | Phase |
|---|---|---|
|
Polycystic Ovary Syndrome Miscarriage Infertility Toxemia Gestational Diabetes |
Drug: metformin |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Efficacy Study |
| Official Title: | Effects of Metformin on Fertility and Pregnancy in Women With Polycystic Ovary Syndrome: a Randomized, Prospective, Placebo-controlled Multicenter Study |
| Estimated Enrollment: | 320 |
| Study Start Date: | August 2002 |
| Estimated Study Completion Date: | December 2009 |
| Estimated Primary Completion Date: | November 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Metformin: Experimental |
Drug: metformin
The obese women will be randomized either to metformin (2g/day) or to placebo, and the non-obese either to metformin (1.5g/day) or to placebo. All subjects will be evaluated 1 to 7 days after spontaneous menstruation (oligomenorrheic patients), or at any other convenient time (amenorrheic subjects). After the treatment of 3 months with metformin/placebo alone, another appropriate infertility treatment will be combined with metformin/placebo (clomiphene, ovulation induction, insemination or in vitro fertilization) if no pregnancy has occurred. This treatment will be continued another 6 months' period. If pregnancy occurs, subjects will be re-examined at 7-8 weeks of gestation.
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Women with PCOS represent about 5-10% of the general female population and one third of the women treated for infertility. Thus, the development of new therapies to improve the efficiency of ovulation induction treatments and the outcome of pregnancy, and to reduce the long-term risks of the syndrome would bring important health benefits.
The central role played by insulin resistance and hyperinsulinemia in PCOS - causing hyperandrogenism, premature follicular atresia, anovulation, oligo-amenorrhea and anovulatory infertility - has led to the use of insulin-lowering drugs for the treatment of this syndrome. The most studied agent is metformin, a biguanide antihyperglycemic drug used to treat Type 2 diabetes mellitus. It has been shown to improve significantly hyperinsulinemia and insulin resistance, to decrease androgen levels, and to improve menstrual pattern and, alone or in addition to clomiphene citrate, to induce ovulation and improve pregnancy rates in women with PCOS in some studies (1,2). Metformin may also decrease risks of early spontaneous miscarriage and gestational diabetes in PCOS (3-6). Two recent RCTs, however, have shown no beneficial effect of metformin compared to placebo as regards rates of pregnancy, miscarriage or life births in women with PCOS (7,8).
Our hypothesis is that metformin may improve pregnancy rates and decrease miscarriage occurrence and complications of pregnancy, such as toxemia and gestational diabetes, in women with PCOS. This multicenter randomized placebo-controlled study is conducted in all five University Hospitals of Finland (Oulu, Kuopio, Helsinki, Tampere and Turku). Blood samples are drawn and the oral glucose tolerance test (OGTT) done before and at 3 months of treatment, after which the treatment with placebo/metformin is continued another 6 months' period together with the appropriate infertility treatment. If pregnancy occurs, the OGTT is done at 7-8 weeks of pregnancy and the placebo/metformin treatment is continued until 12 weeks of pregnancy. The study has already started and is estimated to continue at least until the end of 2009. Power analysis indicated that a minimum of 60 pregnant patients are needed in each group to decrease the risk of miscarriage from 44% to the normal 15%.
Eligibility| Ages Eligible for Study: | 18 Years to 40 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Criteria for PCOS are as defined by ESHRE/ASRM: at least two of the following findings:
Exclusion Criteria:
Contacts and Locations| Finland | |
| University Hopsital of Oulu | |
| Oulu, Finland, 90029 | |
| University Hospital Of Helsinki | |
| Helsinki, Finland | |
| University Hospital of Turku | |
| Turku, Finland | |
| University Hospital of Kuopio | |
| Kuopio, Finland | |
| University Hospital of Tampere | |
| Tampere, Finland | |
| Principal Investigator: | Laure C Morin-Papunen, PhD | University hospital of Oulu |
More Information
| Responsible Party: | Dept of Obstetrics and Gynecology, University Hospital of Oulu ( Laure Morin-Papunen/ Associate Professor ) |
| Study ID Numbers: | T59108 |
| Study First Received: | October 9, 2009 |
| Last Updated: | October 13, 2009 |
| ClinicalTrials.gov Identifier: | NCT00994812 History of Changes |
| Health Authority: | Finland: Ethics Committee |
|
Polycystic ovary syndrome PCOS Metformin |
Miscarriage Infertility Complications of pregnancy |
|
Ovarian Cysts Ovarian Diseases Neoplasms Infertility Pregnancy Complications Gonadal Disorders Physiological Effects of Drugs Diabetes, Gestational Infection Genital Diseases, Female Pathologic Processes Hypoglycemic Agents Syndrome |
Abortion, Spontaneous Disease Metabolic Diseases Metformin Diabetes Mellitus Endocrine System Diseases Cysts Genital Diseases, Male Pharmacologic Actions Toxemia Adnexal Diseases Polycystic Ovary Syndrome Glucose Metabolism Disorders |