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Data Collection Post Radical Prostatectomy

NCT06351579 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2025-09-29

No results posted yet for this study

Summary

The study is designed to collect information on patients undergoing radical prostatectomy (RP), with a primary focus on the occurrence, duration, and severity of post-prostatectomy incontinence. Data will be collected at multiple time points, allowing for a dynamic understanding of urinary incontinence patterns at post RP.

Conditions

  • Stress Urinary Incontinence
  • Radical Prostatectomy
  • BPH

Interventions

OTHER

Control

This is an observational (registry) study for data collection only. No device or intervention will be used in this study.

Sponsors & Collaborators

  • RQM+

    collaborator INDUSTRY

  • Levee Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Bruce Choi · Founder and CTO, Levee Medical, Inc

Eligibility

Min Age
45 Years
Max Age
70 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-30
Primary Completion
2025-07-30
Completion
2025-07-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06351579 on ClinicalTrials.gov