CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,879 enrolled
Drug / intervention
None-observational +3 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02485808
NCT02485808N/ACompleted

Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN) Phenotyping Study Protocol

Arbor Research Collaborative for Health·observational·Posted Jun 30, 2015·Updated Jan 15, 2019

In Brief

An observational study evaluating None-observational, Magnetic Resonance Imaging (MRI), and 2 other interventions for Lower Urinary Tract Symptoms. Completed, enrolled 1,879 participants across 6 sites.

Detailed Summary

The purpose of this study is to advance our understanding of people who experience urinary and bladder problems. We are interested in learning about people's experiences with urinary symptoms and how these symptoms will be managed. We want to understand the important differences among people and what factors affect urinary and bladder problems. After all of the information is collected, we will have a better understanding of how to improve the care and treatment for people who have urinary and bladder problems.

Study Details

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 30, 2015
Enrollment StartApr 1, 2015
Primary CompletionApr 1, 2018
Study CompletionMay 1, 2018
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 11.0 years ago

Interventions

None-observationalother

For surgical patients, follow-up assessments will occur 3 and 12 months after the surgery. For medical patients, follow-up assessments will occur 3 and 12 months after the baseline assessment.

Magnetic Resonance Imaging (MRI)procedure

One time MRI scanning session examining brain structure and function in a resting state and after water consumption.

Multimodal Automated Sensory Testing Systemother

Pressure pain thresholds will be assess using computer-controlled pressures delivered by a device called the Multimodal Automated Sensory Testing System (MAST) device on to the subjects thumbnail bed.

Auditory Sensitivity Testother

Subjects' sensitivity to sound will be evaluated using a series of sounds delivered by a standard audiometer device.