Comparison of diagnostic accuracy of endometrial curettage and aspiration biopsy in patients with endometrial hyperplasia

Phase 3

Recruiting

• Conditions: Endometrial hyperplasia.; Endometrial hyperplasia; N85.0

• Registration Number: IRCT20221008056114N1
• Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 84

Inclusion Criteria

Age 18 to 47 years
Diagnosis of uterine hyperplasia with AUB
Absence of focal lesion

Exclusion Criteria

The patient's unwillingness to participate in the study
Improper use of medication
Presence of focal endometrial lesion
Patient willingness to hysterectomy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
terine hyperplasia. Timepoint: Before treatment. Method of measurement: Curtage.

Secondary Outcome Measures

Name	Time	Method
Endometrial hyperplasia. Timepoint: Three months after treatment. Method of measurement: Sampling of the endometrium and comparison of pathologies.