Overactive Bladder (OAB) Voiding Diary and Urodynamics Correlation Study

NCT ID: NCT03473782

Last Updated: 2023-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

123 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-10-12

Study Completion Date

2023-08-08

Brief Summary

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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

Detailed Description

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Conditions

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Overactive Bladder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Voiding Diary

Voiding Diary

Intervention Type OTHER

A log kept by each patient to record frequency and volume of urine output and fluid input.

Urodynamics Correlation Study

Intervention Type OTHER

Provides patho physiological data by assessing bladder sensation, bladder capacity, the presence of involuntary bladder contractions, bladder compliance and bladder outlet obstruction.

Urodynamics Correlation Study

Voiding Diary

Intervention Type OTHER

A log kept by each patient to record frequency and volume of urine output and fluid input.

Urodynamics Correlation Study

Intervention Type OTHER

Provides patho physiological data by assessing bladder sensation, bladder capacity, the presence of involuntary bladder contractions, bladder compliance and bladder outlet obstruction.

Interventions

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Voiding Diary

A log kept by each patient to record frequency and volume of urine output and fluid input.

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

110 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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NYU Langone Health

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Benjamin Brucker

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

Locations

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New York University School of Medicine

New York, New York, United States

Site Status

Countries

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United States

Other Identifiers

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15-00827

Identifier Type: -

Identifier Source: org_study_id

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