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Clinical and Urodynamic Effects of Minimally Laser (IncontiLaseTM) Procedure for Female Stress Urinary Incontinence

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National Taiwan University

Status and phase

Completed
Phase 4

Conditions

Stress Urinary Incontinence

Treatments

Procedure: the IncontiLaseTM procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT02130375
201402021RINB

Details and patient eligibility

About

The purpose of this study is to get the effect of IncontiLaseTM procedure; and its impact on urinary symptoms and female sexual function.

Full description

To get the objective urodynamic and sonographic effects of IncontiLaseTM procedure on women with stress urinary incontinence; and its impact on urinary symptoms and female sexual function.

Enrollment

35 patients

Sex

Female

Ages

20 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All consecutive sexually active and parous adult women with the complaint of stress urinary incontinence

Exclusion criteria

  • < 20 years old female

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

35 participants in 1 patient group

stress urinary incontinence
Experimental group
Description:
Women with stress urinary incontinence
Treatment:
Procedure: the IncontiLaseTM procedure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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