Skip to main content
Clinical Trials/CTRI/2024/01/061801
CTRI/2024/01/061801
Not yet recruiting
未知

A prospective, interventional, and multi-center study to characterize the efficacy and performance of the 100% Silicone Foley Balloon Catheter 2-way, 100% Silicone Foley Balloon Catheter – BH model 2-way, and 100% Silicone Foley Balloon Catheter – Star/ Ribbed model 2-way - nil

Sterimed Group0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: N00-N99- Diseases of the genitourinary system
Sponsor
Sterimed Group
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Sterimed Group

Eligibility Criteria

Inclusion Criteria

  • 1\.All subjects who undergo urinary catheterization indicated for long term catheterization of minimum of 30 days
  • 2\.Both Male and Female patients will be enrolled
  • 3\.All patients who are willing to provide informed consent for participation in the study

Exclusion Criteria

  • 1\.Subjects not suitable for intervention with silicone Foley catheter
  • 2\.All subjects who are not willing to provide informed consent for participation in the study
  • 3\.Pediatric population
  • 4\.Neurogenic bladder condition subjects
  • 5\.Immobilized subjects
  • 6\.Subjects having urethral strictures

Outcomes

Primary Outcomes

Not specified

Similar Trials