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Clinical Trials/NCT05901948
NCT05901948CompletedNot Applicable

Asherman Syndrome: Pre-surgical Grading to Improve Gauge Prognostic Values and Improve Outcomes

Ebtesama Hospital1 site in 1 country65 target enrollmentStarted: January 7, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
65
Locations
1
Primary Endpoint
Percentage Resumption of normal cavity on hystero-salpingography

Study Overview

Brief Summary

Utilising a novel pre-surgical grading system to class cases of asherman syndrome into 3 groups based on expected difficulty of surgery and potential prognostic outcomes.

Detailed Description

Using the grading system, patients are classified into Mild, Moderate and Severe Asherman Syndrome. With the mild disease having the best prognostic value and a 1 step procedure, Moderate cases having a mediocre prognosis and usually multi-step procedure and Severe cases having a poor prognosis and counseled to other options. This observational study looks at the surgical outcomes following hysteroscopy for cases graded according to the new system to identify the accuracy of the classification in predicting the surgical success and prognostic value.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

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

Inclusion Criteria

  • Asherman Syndrome
  • intra-uterine synechiae

Exclusion Criteria

  • patients with a fundectomy or uterine reduction surgery.

Outcomes

Primary Outcomes

Percentage Resumption of normal cavity on hystero-salpingography

Time Frame: 1 month

assessing the improvement of the cavity of the uterus in hystero-salpingography

Secondary Outcomes

  • Menses(3 months)

Investigators

Sponsor
Ebtesama Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yehia Shawki

Endoscopy unit director

Ebtesama Hospital

Study Sites (1)

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