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NCT06209333: OABS/BT/PFET

Effect of BT and PFET on Urinary Symptoms and Quality of Life in Patients With OABS

Status unknown NA Last updated 17 January 2024
What this trial tests

NA trial testing Standard Patient Education in Overactive Bladder Syndrome (OABS) in 50 participants. Status unknown.

Timeline
15 October 2023
Primary endpoint
15 October 2024
15 October 2024

Quick facts

Lead sponsorHacettepe University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment50
Start date15 October 2023
Primary completion15 October 2024
Estimated completion15 October 2024
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Hacettepe University

Who can join

18 and older, any sex, with Overactive Bladder Syndrome (OABS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study was to examine the effects of bladder training and pelvic floor exercise training programs given in addition to Botulinum Toxin-A (BTx-A) application on urinary symptoms and quality of life in patients with Overactive Bladder Syndrome (AAMS) who do not respond to conservative treatments. Individuals who meet the criteria for inclusion in the study and agree to participate in the study will be divided into 2 separate research branches.The patients to be included in the study will be divided into two groups as "Group 1=Botox + physiotherapy " or "Group 2=Botox group ". In addition to the BTx-A application, bladder training and pelvic floor exercise training will be applied to patients in the first group, while standard patient training will be provided to patients in the second group. Severity of urinary symptoms, quality of life and subjective perception of improvement Before BTx-A application, 2 weeks and 12 weeks after BTX-A application, International Incontinence Consultation Questionnaire - Women's Lower Urinary Tract Symptoms (ICIQ-FLUTS), 1-hour ped test, International Incontinence Consultation- Lower Urinary Tract Symptoms Quality of Life Scale (ICIQ-LUTS) and Global Perception of Improvement will be evaluated.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Standard Patient Education

Trials testing the same drug.

Other Hacettepe University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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