Last updated: April 25, 2025
Sponsor: Cairo University
Overall Status: Active - Recruiting
Phase
N/A
Condition
Genitourinary Prolapse
Enuresis
Urinary Incontinence
Treatment
Bladder distension group
Empty bladder group
Clinical Study ID
NCT06642311
Anteflexion /hysteroscoy
Ages 18-60 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients with excessive anteflexion of the uterus
Exclusion
Exclusion Criteria:
Cervical pathology
Previous cervical surgery
Severe vaginal bleeding
Study Design
Total Participants: 48
Treatment Group(s): 2
Primary Treatment: Bladder distension group
Phase:
Study Start date:
October 30, 2024
Estimated Completion Date:
April 30, 2025
Connect with a study center
Obstetrics &Gynecology Department , Faculty of medicine ,Cairo university
Cairo,
EgyptActive - Recruiting
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