Trial · NCT07899450
Comparison of Two Autologous Sling Procedures for Stress Urinary Incontinence in Women
NCT07899450, Not applicable, Completed, Mohamed Ehab Saad Fadl
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Two Autologous Sling Procedures for Stress Urinary Incontinence in Women. Trials, record NCT07899450. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07899450
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Two Autologous Sling Procedures for Stress Urinary Incontinence in Women
- NCT number
- NCT07899450
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 40 participants, actual
- Lead sponsor
- Mohamed Ehab Saad Fadl
- Conditions
- Stress Urinary Incontinence (SUI)
- Interventions
- Transobturator Autologous Vaginal Wall Sling, Autologous Rectus Sheath Pubovaginal Slinge
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Percentage of Participants With Objective Cure on Cough Stress Testing | 6 months after surgery | Objective cure is defined as the absence of visible urine leakage during a standardized cough stress test at the six-month postoperative assessment. Participants with visible urine leakage during the test are classified as treatment failures. |
| Secondary | Change in ICIQ-UI Short Form Score | Baseline and 6 months after surgery | Change from baseline in the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) total score. Scores range from 0 to 21, with higher scores indicating greater urinary incontinence severity and impact. A decrease indicates improvement. |
| Secondary | Operative Time | During surgery | Duration of the surgical procedure, measured in minutes. |
| Secondary | Percentage of Participants With Postoperative Complications | From surgery through 6 months after surgery | Percentage of participants experiencing postoperative complications, with complications classified according to the Clavien-Dindo classification. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07899450
GET https://conductscience.org/api/trials/v1/NCT07899450/registered