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The effect of letrosol on endometrial histology in patients with Disordered prolifrative endometrium or Simple hyperplasia

The effect of letrosol on endometrial histology in patients with Disordered prolifrative endometrium or Simple hyperplasia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012092310901N2
Enrollment
92
Registered
2012-11-13
Start date
2012-08-22
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

endometrial disorders. malignant neoplasm of female genital organs

Interventions

Intervention 1: Intervention: letrozol, tablet 2.5 mg, one time daily, three months. Intervention 2: Control group: routin treatment, megestrol, tablet 40mg, three months.
Treatment - Drugs
Intervention: letrozol, tablet 2.5 mg, one time daily, three months
Control group: routin treatment, megestrol, tablet 40mg, three months

Sponsors

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

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- Women with Abnormal Uterine Bleeding and Disordered proliferative endometrium or Simple hyperplasia; 2- the desire to participate in the study. Exclusion criteria: 1- persons sensitive to letrozole; 2- Severe impairment of liver function; 3- uncontrolled hypertension; 4- thromboembolism

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Endometrial histology. Timepoint: before intervention, three months after intervention. Method of measurement: endometrial biopsia.

Secondary

MeasureTime frame
Flashing. Timepoint: during 3 months. Method of measurement: questionnaire.;Chest pain & dyspnea. Timepoint: during three months. Method of measurement: questionnaire.;Headeche. Timepoint: during 3 months. Method of measurement: questionnaire.;Insomnia. Timepoint: during 3 months. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Parvin Mostafa Gharebaghi

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

gharabagh.p@tbzmed.ac.ir+98 41 1553 9161

Outcome results

None listed

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