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Trial · NCT07899268

Continence Post Retzius-Sparing Versus Standard Robot-Assisted Radical Prostatectomy

NCT07899268, Not applicable, Completed, Armed Forces College of Medicine, Cairo, Egypt

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Continence Post Retzius-Sparing Versus Standard Robot-Assisted Radical Prostatectomy. Trials, record NCT07899268. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07899268

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Continence Post Retzius-Sparing Versus Standard Robot-Assisted Radical Prostatectomy
NCT number
NCT07899268
Status
Completed
Phases
Not applicable
Enrollment
88 participants, actual
Lead sponsor
Armed Forces College of Medicine, Cairo, Egypt
Conditions
Radical Prostatectomy, Robotic Radical Prostatectomy, Retzius-sparing Robot-assisted Radical Prostatectomy With "Sandwich" Technique of Total Urethral Reconstruction
Interventions
Procedure: Retzius-Sparing Robot-Assisted Radical Prostatectomy (RS-RARP), Standard Robot-Assisted Radical Prostatectomy (S-RARP)
First posted
2026-10-27
Last updated
2026-11-12

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryUrinary Continence (0-1 pads/day)1 week after catheter removalThe proportion of patients who achieve urinary continence (defined as the need for 0-1 pad per day) within a specified postoperative period e.g., 7 days or 30 days or 3 months.
SecondaryContinence at 1 and 3 months1 and 3 months after catheter removalICIQ-UI score at 1 month and 3 months after catheter removal
SecondaryAssessing positive surgical margins1 week and 3 monthsAssessment of PSMs postoperatively to assess the oncological outcomes and assessment of PSA level at 3 months

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.

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
12011718BACKGROUNDPubMed
20828236BACKGROUNDPubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07899268

GET https://conductscience.org/api/trials/v1/NCT07899268/registered