Patients with abnormal uterine bleeding and have disordered proliferative or hyperplastic endometrium with or without atypia. Endometrial glandular hyperplasia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients with abnormal uterine bleeding and havingdisordered proliferative or hyperplastic endometrium with or without atypia. Consent to participate. Exclusion criteria: Patients who have allergy to metformin, Patients with renal failure, nausea, vomiting, anorexia, anemia, cutaneous lesionsor not satisfied to participate in the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endometrialpathology. Timepoint: before surgery. Method of measurement: Pathologic assessment.;Endometrial Histologic type. Timepoint: Three months after medical therapy. Method of measurement: Microscopic assessment. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences