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Polymer used in the Treatment of Stress Incontinence in Women.

Polysacaride Gel for Treating Stress Urinary Incontinece in Women.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-46xb4bm
Enrollment
Unknown
Registered
2021-04-05
Start date
2017-03-15
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary incontinence

Interventions

General hasn't points
A total of 15 patients were eligible for the study and underwent the following procedures in a single moment: Application of the cellulose polysaccharide gel with a concentration of 0.8% was performed

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Universidade Federal de Pernambuco
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Reduction of urinary loss on exertion, verified through the ICIQ-SF; 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. The Quality of Life (QOL) questionnaire at the time of the intervention indicated that all patients reported a better quality of life (62.5%). 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.

Countries

Brazil

Contacts

Public ContactFernanda Calisto
fernandacamilacalisto@gmail.com+55 (81) 99954-6898

Outcome results

None listed

Source: REBEC (via WHO ICTRP)