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

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01279512
Enrollment
50
Registered
2011-01-19
Start date
2006-12-31
Completion date
2008-12-31
Last updated
2012-01-06

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

Conditions

PCO

Keywords

Metformin Acarbose pco infertility overweight

Brief summary

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

Detailed description

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.

Interventions

DRUGMetformin

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.

DRUGAcarbose

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).

Sponsors

Royan Institute
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Weight reduction (BMI improvement)After 3 months of Metformin or Acarbosecompare the effect of Metformin and Acarbose to weight reduction

Secondary

MeasureTime frameDescription
FSH6 monthscompare the effect of Metformin and Acarbose to decrease the level of FSH
LH6 monthscompare the effect of Metformin and Acarbose to decrease the level of LH
Estradiol6 monthscompare the effect of Metformin and Acarbose to decrease the Esteradiol level
Prolactin6 monthscompare the effect of Metformin and Acarbose to decrease the Prolactin level
Fasting blood sugar (FBS)two hours post prandial blood sugarCompare the effect of Metformin and acarbose to fasting blood sugar reduction
Total cholesterol6 monthscomparethe the effect of Metformin and Acarbose to decrease total cholesterol level
triglyceride6 monthscomparethe the effect of Metformin and Acarbose to decrease the triglyceride level
High density Lipoprotein6 monthscompare the the effect of Metformin and Acarbose to decrease high density lipoprotein
Low density lipoprotein6 monthscompare the the effect of Metformin and Acarbose to decrease Low Density Lipoprotein
Total testosterone6 monthscompare the the effect of Metformin and Acarbose to decrease Total testosterone level

Countries

Iran

Outcome results

None listed

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