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Clinical Trials/NCT07309692
NCT07309692
Recruiting
Not Applicable

Three Dimensional Ultrasonography Versus Hysteroscopy for the Evaluation of Patients With Perimenopausal Bleeding

Sohag University1 site in 1 country106 target enrollmentStarted: December 1, 2025Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
106
Locations
1
Primary Endpoint
The sensitivity and specificity of the 3D ultrasonography for the diagnosis of the causes of peri-menopausal bleeding as compared to hysteroscopy

Overview

Brief Summary

The study aims to compare between 3D ultrasonography and hysteroscopy for the evaluation of cases with Peri-menopausal bleeding

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
40 Years to 55 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Any pattern of abnormal uterine bleeding as menorrhagia or metrorrhagia for more than 3 months at age between 40 and 55 years , and no ovarian lesion or local cause of bleeding as vaginal or cervical ulcer

Exclusion Criteria

  • • Women with postmenopausal bleeding.
  • Systemic causes of perimenopausal bleeding DM Hypertension or chronic liver disease.
  • Women on hormonal therapy or using any contraception as IUD.
  • Women have contraindication for hysteroscopy as cervical stenosis or pregnancy.

Outcomes

Primary Outcomes

The sensitivity and specificity of the 3D ultrasonography for the diagnosis of the causes of peri-menopausal bleeding as compared to hysteroscopy

Time Frame: 9 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Abd Al Rahim Fattouh

Resident doctor at obstetric and gynecology department of sohag university

Sohag University

Study Sites (1)

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