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Histopathological Diagnosis of Adenomyosis

W

Woman's Health University Hospital, Egypt

Status

Completed

Conditions

Adenomyosis

Treatments

Procedure: hysteroscopic endo-myometrial biopsy
Device: ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT02340533
AD0152015

Details and patient eligibility

About

The purpose of this study is to develop and evaluate a hysteroscopic endo-myometrial biopsy for diagnosing adenomyosis.

Enrollment

200 estimated patients

Sex

Female

Ages

38 to 52 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • females complaining of pelvic congestion: dysmenorrhea, dyspareunia, chronic pelvic pain, menorrhagia, metrorrhagia

Exclusion criteria

  • refusal of the patient to get enrolled in the study

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

Single Blind

200 participants in 1 patient group

adenomyosis
Experimental group
Description:
females attending the gynecology outpatient clinic complaining of chronic pelvic congestion will get enrolled in the study. Two dimensional ultrasonography will be performed to asses the presence or absence of adenomyosis or any associated lesions. All the patients were then be subjected to office hysteroscopy and endo-myometrial biopsies will be taken. Histopathological examination of the samples will then be done. From these recruited patients, some will be indicated to perform hysterectomy. The final diagnosis will then be based on the histopathological examination of the specimen retrieved from hysterectomy. The accuracy of the ultrasound and the hysteroscopic endo-myometrial biopsy will then be compared and assessed.
Treatment:
Device: ultrasound
Procedure: hysteroscopic endo-myometrial biopsy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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