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

Questionnaire About The Incidence of Lower Urinary Tract Symptoms Among a Sample of Women Before and After Surgical Correction of Uterine Prolapse and Impact on Quality of Life

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06260436
Enrollment
180
Registered
2024-02-15
Start date
2021-05-30
Completion date
2024-12-30
Last updated
2024-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse

Brief summary

. 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.

Detailed description

Pelvic organs prolapse (POP) is defined as the downward descent of the pelvic organs resulting in protrusion of the vagina and/or uterine cervix. POP and overactive bladder (OAB) often co-exist. The International Continence Society defines OAB as urgency with or without urge incontinence, usually with frequency and nocturia Of women with symptomatic pelvic organ prolapse, 13-39% experience voiding dysfunction (VD). The aim of the study is to determine the effect of prolapse surgery on voiding function. 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. Non-responders will send a reminder after three weeks and if the non-responders still failed to respond were eventually asked to complete a short form comprising questions on urgency and incontinence. This procedure followed guidelines outlined by the local ethical committee. 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. stress incontinence according to the International Continence Society defined as leakage caused by exertion (coughing or sneezing, moving, or lifting) and urge incontinence as leakage associated with urgency.

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age; greater than or equal to 18 years 2. women with urogenital prolapse grade 3 or more 3. indicated for surgical repair for pelvic organ prolapse 4. Willing and able to sign an informed consent 5. Willing to comply with the study protocol

Exclusion criteria

1. Anti-incontinence surgery 2. Lower urinary tract anomaly 3. Active urinary tract infections 4. Bladder tumor. 5. Bladder stones

Design outcomes

Primary

MeasureTime frameDescription
effect of surgical correction of pelvic organ prolapse on the lower urinary tract symptoms3 monthsthe effect of surgical correction of pelvic organ prolapse on the lower urinary tract symptoms will be checked through a validated questionnaire before and after surgical correction

Secondary

MeasureTime frameDescription
effect of surgical correction of pelvic organ prolapse on the quality of life3 monthsthe questionnaire will check the effect of surgical correction of pelvic organ prolapse on quality of life

Countries

Egypt

Contacts

Primary Contacttharwat gl mohammed
tharwat.fares3@gmail.com01151166826
Backup Contacttharwat gl mohamed
tharwat.fares3@gmail.com01151166826

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026