Women With Asymptomatic Endometrial Hyperplasia

Completed

• Conditions: Endometrial Hyperplasia

• Registration Number: NCT02100137
• Lead Sponsor: Medical University of Vienna

Brief Summary

The purpose of this study is to evaluate the clinical meaning of an endometrial hyperplasia diagnosed using a vaginal ultrasound during routine gynecological examination.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-09
• Primary Completion: 2010-11
• Study First Submitted: 2012-03-05
• Study Completion: 2012-07
• Status Verified: 2014-03
• Study First Submitted QC: 2014-03-26
• Last Update Submitted: 2014-03-26
• Study First Posted: 2014-03-31
• Last Update Posted: 2014-03-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 1000

Inclusion Criteria

• asymptomatic women with endometrial hyperplasia diagnosed using a vaginal ultrasound

Exclusion Criteria

• postmenopausal bleeding

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Number of invasive endometrial cancers	Participants will be followed for the duration of hospital and until the results of the final histology from the endometrial biopsy are completed, for an expected average of 10 days

Secondary Outcome Measures

Name	Time	Method
Number of women with atypical endometrial hyperplasia	Participants will be followed for the duration of hospital and until the results of the final histology from the endometrial biopsy are completed, for an expected average of 10 days

Trial Locations

Locations (1)

Medical University of Vienna; 🇦🇹 Vienna, Austria