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OpenTrials
Completed

NCT Number: NCT02340533

Histopathological Diagnosis of Adenomyosis

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

Completed

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Key information

Age range

38 year–52 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Kasr el aini hospital

Cairo, Cairo Governorate, 12211, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

hysteroscopic endo-myometrial biopsy

Procedure

Ultrasound

Device

two dimensional trans-vaginal ultrasonography

Primary outcomes

  1. Number of participants with diagnosis of adenomyosis cases

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Woman's Health University Hospital, Egypt

Other

Registry information

Official study title

The Diagnostic Accuracy of Hysteroscopic Endomyometrial Biopsy in Adenomyosis

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jan 16, 2015
Registry last updated
Jul 28, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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