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NCT03473782 Clinical Trial

Overactive Bladder (OAB) Voiding Diary and Urodynamics Correlation Study

Overactive Bladder Clinical Trial

Official title:
Overactive Bladder (OAB) Voiding Diary and Urodynamics Correlation Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03473782
Other study ID # 15-00827
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 12, 2015
Est. completion date August 8, 2023

Study information
Verified date August 2023
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a prospective cohort study study with the primary aim of identifying the strongest correlating parameters between voiding diaries and UDS studies most predictive for each type of urologic condition. Investigators will focus on OAB related conditions, as these are symptoms

Recruitment information / eligibility
Status Completed
Enrollment 123
Est. completion date August 8, 2023
Est. primary completion date August 8, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 110 Years
Eligibility Inclusion Criteria: - completing a bladder diary - undergoing VUDS Exclusion Criteria: - have a urinary tract infection - neurogenic bladder - history of pelvic irradiation - prolapse alone without LUTS - pregnant - incarcerated - hospital employee - unable to give consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Voiding Diary
A log kept by each patient to record frequency and volume of urine output and fluid input.
• Urodynamics Correlation Study
Provides patho physiological data by assessing bladder sensation, bladder capacity, the presence of involuntary bladder contractions, bladder compliance and bladder outlet obstruction.

Locations
Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)
Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measure of urgency incontinence using Voiding Diary patients will record urgency in diary 60 Months
See also
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Completed NCT01458197 - A Phase 2 Study to Compare the Efficacy and Tolerability of Tarafenacin 0.2 mg and Tarafenacin 0.4 mg to Placebo in Patients Suffering From Overactive Bladder. Phase 2
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Terminated NCT01758848 - Physical Therapy for Overactive Bladder N/A
Terminated NCT01003249 - Dysfunctional Voiding and Lower Urinary Tract Symptoms With Baclofen Phase 4