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NCT06260436

Questionnaire of Lower Urinary Tract Symptoms Among Women Before and After Surgical Correction of Uterine Prolapse

Status unknown Last updated 21 February 2024
What this trial tests

trial in Pelvic Organ Prolapse in 180 participants. Status unknown.

Timeline
30 May 2021
Primary endpoint
30 September 2024
30 December 2024

Quick facts

Lead sponsorAssiut University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment180
Start date30 May 2021
Primary completion30 September 2024
Estimated completion30 December 2024
Sites1 location across Egypt

Conditions studied

Sponsor

Assiut University

Who can join

18 and older, female only, with Pelvic Organ Prolapse. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

. The study will include patients who underwent Pelvic reconstructive surgery for advanced pelvic organ prolapse (POP-Q ≥ 3). Data regarding preoperative evaluation, surgical procedure, and post-operative management will be collected. women will receive a follow up questionnaire. . The baseline questionnaire included data on age, urinary incontinence, daytime frequency, nocturia, postmicturition dribble, straining, urgency, incomplete bladder emptying, and hesitancy. Women were asked about leakage caused by coughing or sneezing, moving, lifting, sleeping, sexual intercourse, urgency, and rest.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pelvic Organ Prolapse

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06260436.

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