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Completed

NCT Number: NCT01279512

Metformin Versus Acarbose Treatment in Infertile Overweight Women With Polycystic Ovary Syndrome (PCOS)

This study is a prospective randomized clinical trial to compare the endocrine and metabolic effects of two anti diabetic drugs (metformin vs. acarbose) in infertile overweight women with PCOS

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Key information

Conditions

PCO

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Royan Institute

Tehran, Iran

About this study

This study is a prospective randomized clinical trial to compare the endocrine and metabolic effects of two anti diabetic drugs (metformin vs. acarbose) in infertile overweight women with PCOS.

Polycystic ovary syndrome (PCOS) is characterized by menstrual irregularity, hyperandrogenism, chronic anovulation and enlarged ovaries with more than twelve peripherally located follicles less than 10 mm in diameter. Hyperinsulinemia is one of the diagnostic features of PCOS and patients with PCOS are found to have resistance to either endogenous or exogenous insulin. Different insulin sensitizing drugs used for improvement of hyperinsulinemia in PCOS subjects. Metformin (N dimethyl-biguanide) is an anti diabetic drug that increases glucose utilization in insulin sensitive tissues. Acarbose is an alfa-Glycosidase inhibitor acts by slowing the absorption of carbohydrates from the intestine, prevents Glucosidase activity in the brush-border of the intestinal mucosa, decreasing disaccharide digestion, reducing enteric monosaccharide absorption, so minimizing the postprandial rise of blood glucose concentration. The aim of present study is to compare the endocrine and metabolic effects of these two antidiabetic drugs (metformin vs. acarbose) in infertile overweight women with PCOS.

The study population comprises all infertile patients with diagnosis of polycystic ovarian syndrome who were overweight (BMI>25Kg/m2). The PCO subjects will be recognized based on the Rotterdam criteria inclusive 1) irregular menstruation, 2) clinical and /or biochemical signs of hyperandrogenism, 3) polycystic ovaries (presence of 12 or more follicles in each ovary measuring 2-9 mm in diameter, and /or increased ovarian volume greater than 10 ml). Diagnosis of PCOS was confirmed by the presence two of three criteria beside the infertility.

In this study all eligible patients will be randomly allocated into two study groups by a computerized randomization method:

Acarbose group will be treated by acarbose (its dose will be 100 mg/day in the first week, 200 mg/ day in the second week and 300 mg/ day for the next 10 weeks). Metformin group will be received metformin. The metformin dose will be 500 mg/ day in the first week, 1000 mg/ day in the second week and 1500 mg/ day for the next 10 weeks.

Data collection will be performed by using questionnaire to be filled as per the available records and laboratory results. This study will be accomplished in Royan Institute on 50 PCO patients (25 patients in each group) and a continuous sampling method will be applied. Data analysis will be done through descriptive and perceptive statistical methods by using SPSS software version 15 for windows.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Poly Cystic Ovarian Syndrome patients
  • Age < 40 years
  • BMI > 25 kg/m2

Exclusion criteria

  • Smoking
  • Overt diabetes mellitus, hyperprolactinemia, diseases that would disturb clinical and hormonal responses (adrenal disease or tumors, ovarian tumors, thyroid disease)
  • The use of hormonal medications or drugs that might interfere with carbohydrate metabolism over the last 6 months.

Treatment and study plan

metformin

Drug

The metformin dose will be 500 mg/ day in the first week, 1000 mg/ day in the second week and 1500 mg/ day for the next 10 weeks.

Other names: Metformin description

Acarbose

Drug

Acarbose group will be treated by acarbose (its dose will be 100 mg/day in the first week, 200 mg/ day in the second week and 300 mg/ day for the next 10 weeks).

Other names: Acarbose description

Primary outcomes

  1. Weight reduction (BMI improvement)

    Time frame: After 3 months of Metformin or Acarbose

    compare the effect of Metformin and Acarbose to weight reduction

Secondary outcomes

  1. Fasting blood sugar (FBS)

    Time frame: two hours post prandial blood sugar

    Compare the effect of Metformin and acarbose to fasting blood sugar reduction

  2. FSH

    Time frame: 6 months

    compare the effect of Metformin and Acarbose to decrease the level of FSH

  3. LH

    Time frame: 6 months

    compare the effect of Metformin and Acarbose to decrease the level of LH

  4. Estradiol

    Time frame: 6 months

    compare the effect of Metformin and Acarbose to decrease the Esteradiol level

  5. Prolactin

    Time frame: 6 months

    compare the effect of Metformin and Acarbose to decrease the Prolactin level

  6. Total testosterone

    Time frame: 6 months

    compare the the effect of Metformin and Acarbose to decrease Total testosterone level

  7. Total cholesterol

    Time frame: 6 months

    comparethe the effect of Metformin and Acarbose to decrease total cholesterol level

  8. triglyceride

    Time frame: 6 months

    comparethe the effect of Metformin and Acarbose to decrease the triglyceride level

  9. High density Lipoprotein

    Time frame: 6 months

    compare the the effect of Metformin and Acarbose to decrease high density lipoprotein

  10. Low density lipoprotein

    Time frame: 6 months

    compare the the effect of Metformin and Acarbose to decrease Low Density Lipoprotein

Sponsors and collaborators

Lead sponsor

Royan Institute

Other Gov

Registry information

Official study title

Metformin vs. Acarbose Treatment in Infertile Overweight Women With PCOS: A Prospective Randomized Clinical Trial

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Jan 19, 2011
Registry last updated
Jan 6, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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