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Treatment of endometrial thickness with metformin and progesterone

Phase 3
Conditions
Endometrial hyperplasia.
Endometrial hyperplasia
N85.0
Registration Number
IRCT20230128057254N1
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

Endometrial hyperplasia confirmed by endometrial biopsy
Absence of liver and kidney disease
Consent to participate in the study

Exclusion Criteria

Use of metformin within the last 6 months
Impaired liver and kidney tests
Diabetics treated with insulin
Postmenopausal women
Intolerance to metformin side effects

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Endometrial hyperplasia. Timepoint: 3 months and 6 months after intervention initiation. Method of measurement: Endometrial curettage.
Secondary Outcome Measures
NameTimeMethod
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