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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05493748
Other study ID # # 6237 PRIISA 6017
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 1, 2022
Est. completion date December 31, 2023

Study information

Verified date August 2022
Source Hospital Italiano de Buenos Aires
Contact Agustina Vendramini, Dra.
Phone 5491123950443
Email agustina.vendramini@hiba.org.ar
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

According to International Urogynecological Association and International Continence Society joint report on the terminology for female pelvic floor dysfunction, overactive bladder syndrome (OAB) is defined as urinary urgency, usually accompanied by frequency and nocturia, with or without urgency urinary incontinence, in the absence of urinary tract infection or other obvious pathology. Bladder training lasting for a minimum of 4 to 6 weeks is indicated as a first-line treatment. The investigators' goal is to compare changes in satisfaction, measured in terms of quality of life, in 2 groups of women with different main accompanying symptoms in OAB (frequency vs. nocturia), before and after bladder training utilizing telemedicine (virtual bladder training), for 4 to 6 weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 86
Est. completion date December 31, 2023
Est. primary completion date October 31, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - women over 18 years of age - Live in Buenos Aires City - Overactive Bladder Syndrome - Access to virtual appointment Exclusion Criteria: - Previous overactive bladder syndrome treatment. - Prior stress urinary incontinence or pelvic organ prolapse surgery. - History of Neurogenic Bladder, pelvic organs prolapse or pelvic radiation. - Pregnancy.

Study Design


Intervention

Other:
Bladder training
Bladder training for overactive bladder syndrome.

Locations

Country Name City State
Argentina Hospital Italiano de Buenos Aires Buenos Aires

Sponsors (1)

Lead Sponsor Collaborator
Hospital Italiano de Buenos Aires

Country where clinical trial is conducted

Argentina, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in King's Health Questionnaire (KHQ) score KHQ score: 0-100 points per domain. Higher scores mean a worse outcome.Ten points change in KHQ score, before and after bladder training. Change from Baseline King's Health Questionnaire at 6 weeks
Primary Change in International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) score ICIQ SF score: 0-21 points. Higher scores mean a worse outcome. Three points change in ICIQ-SF score, before and after bladder training. Change from Baseline International Consultation on Incontinence Questionnaire Short Form at 6 weeks
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