Polymer used in the Treatment of Stress Incontinence in Women.

Not Applicable

• Conditions: rinary incontinence; urine leaks.; N39.3

• Registration Number: RBR-46xb4bm
• Lead Sponsor: niversidade Federal de Pernambuco

Brief Summary

The study considered as primary outcome the improvement or disappearance of symptoms after six months of intervention. Post-intervention Quality of Life (QOL) questionnaire indicated that all of these patients related a better quality of life (62.5 %).

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-03-28
• Study Start: 2021-04-05
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Data analysis completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Female volunteers; diagnosis of stress urinary incontinence; no history of previous surgery.

Exclusion Criteria

Volunteers with previous diagnosis of infravesical obstruction of a mechanical nature; previous diagnosis of neurogenic bladder, presence of urethral hypermobility.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of urinary loss on exertion, verified through the ICIQ-SF;<br>PAD-Test Quality of Life questionnaire, after analyzing the results in the pre and post-intervention moments.;Significant improvement and disappearance of urinary loss symptoms six months after the intervention. <br>The Quality of Life (QOL) questionnaire at the time of the intervention indicated that all patients reported a better quality of life (62.5%). <br>Through the PAD-test it was possible to observe a decrease in urinary loss of 85% comparing the pre and post-intervention results (BCA - Bacterial Cellulose Application) with a p-value equal to 0.000009.