Patients with abnormal bleeding and endometrial proliferative and Hayprplastyk with irregular glands with and 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 |
|---|---|
| Endometrial pathology. Timepoint: Before surgery. Method of measurement: Pathological evaluation.;Histologic types of endometrial. Timepoint: Three months after the first dose. Method of measurement: Microscopic examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University Of Medical Sciences