CTRI/2022/04/042235
Not yet recruiting
Phase 4
A prospective, observational and multi-center study to characterize the safety, efficacy and performance of the LATEX FOLEY BALLOON CATHETER (2-WAY & 3-WAY)
STERIMED MEDICAL DEVICES PVT LTD0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: N394- Other specified urinary incontinence
- Sponsor
- STERIMED MEDICAL DEVICES PVT LTD
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All subjects who undergo urinary catheterization.
- •\-Both Male and Female patients will be enrolled.
- •\-Patients who have been treated with LATEX FOLEY BALLOON CATHETER (2WAY \& 3\-WAY)
- •\-All patients who are willing to provide informed consent for participation in the study
Exclusion Criteria
- •\-Subjects not suitable for intervention with LATEX FOLEY BALLOON CATHETER (2\-WAY \& 3\-WAY).
- •\-All subjects who are not willing to provide informed consent for participation in the study
- •\-Subjects having allergy to Latex
- •\-Subjects using silicone foley catheter
Outcomes
Primary Outcomes
Not specified
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