MedTrace Logo

Postoperative Patient Comfort and Quality of Micturition in Suprapubic Tube vs. Transurethral Catheterization After RARP

NCT02812173 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 234

Last updated 2022-12-07

No results posted yet for this study

Summary

The purpose of the study is to determine, whether the postoperative quality of micturition and continence can be improved depending on the urinary drainage catheter and retention after robot assisted radical prostatectomy. Another finding could be the study of the pain assessment of the patient, as well as the pain medication at the various derivatives. Further check whether infections and the presence of bacteriuria can be reduced or avoided by the form of urinary drainage.

Conditions

Interventions

DEVICE

suprapubic tube ex 2 day

balloon catheter for suprapubic bladder-drainage, suprapubic tube removal on the second day after the surgery

DEVICE

suprapubic tube ex 5 day

balloon catheter for suprapubic bladder-drainage, suprapubic tube removal on the fifth day after the surgery

DEVICE

transurethral catheter ex 5 day

transurethral catheter withdrawal removal on the fifth day after the surgery

Sponsors & Collaborators

  • St. Antonius Hospital Gronau

    lead OTHER

Principal Investigators

  • Nina Harke, MD. · St. Antonius Hospital Gronau

  • Mustapha Addali, MD. · St. Antonius Hospital Gronau

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-07-31
Completion
2018-06-30

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

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 NCT02812173 on ClinicalTrials.gov