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Comparing the effect of Metformin and Megestrol acetate on endometrial histology in patients with disordered proliferative or hyperplastic endometrium. A RCT

Comparing the effect of Metformin and Megestrol acetate on endometrial histology in patients with disordered proliferative or hyperplastic endometrium. A RCT

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205265283N4
Enrollment
90
Registered
2013-03-16
Start date
2011-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Patients with abnormal uterine bleeding and have disordered proliferative or hyperplastic endometrium with or without atypia. Endometrial glandular hyperplasia

Interventions

Intervention 1: First group: fifteen cases with disordered proliferative endometrium , 15 cases with hyperplastic atypical endometrium and 15 cases with hyperplasticendometrium and without atypia who
Treatment - Drugs
First group: fifteen cases with disordered proliferative endometrium , 15 cases with hyperplastic atypical endometrium and 15 cases with hyperplasticendometrium and without atypia who referred to Al
Second group: fifteen cases with disordered proliferative endometrium , 15 cases with hyperplastic atypical endometrium and 15 cases with hyperplastic endometrium and without atypia who referred to

Sponsors

Women's Reproductive Health Research Center, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 60 Years

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

MeasureTime 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

Public ContactManizheh Sayyah-Melli

Tabriz University of Medical Sciences

manizheh.sayyahmelli@gmail.com+98 41 1553 9161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026