Questionnaire on urinary symptoms in women before and after prolapse surgery
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
This study is testing how pelvic surgery affects urinary symptoms in women with pelvic organ prolapse by asking them questions before and after the surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 180 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Assiut, Assuit) |
| Trial ID | NCT06260436 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the impact of pelvic reconstructive surgery on urinary function in women with advanced pelvic organ prolapse. Participants will complete a baseline questionnaire covering various urinary symptoms and will receive follow-up questionnaires post-surgery to evaluate changes in their condition. The study will collect data on preoperative evaluations, surgical procedures, and postoperative management to understand the effects of surgery on voiding dysfunction. Non-responders will be reminded to participate to ensure comprehensive data collection.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and older with grade 3 or higher urogenital prolapse who are indicated for surgical repair.
Not a fit: Patients who have undergone anti-incontinence surgery, have lower urinary tract anomalies, active urinary tract infections, bladder tumors, or bladder stones may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into how surgical correction of uterine prolapse affects urinary symptoms, potentially improving patient outcomes.
How similar studies have performed: While similar studies have explored the relationship between pelvic organ prolapse and urinary symptoms, this specific approach focusing on postoperative outcomes is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Assiut, Assuit
- Assuit University — Assiut, Assuit, Egypt (Recruiting)
Study contacts
- Principal investigator: tharwat gm mohamed — Assiut University
- Study coordinator: tharwat gl mohammed
- Email: tharwat.fares3@gmail.com
- Phone: 01151166826
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.