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Patient Satisfaction of Virtual vs In-Person Workup and Treatment of Lower Urinary Tract Symptoms.

StatusSuspended
PhaseNot applicable
Started2022-08-30
View on ClinicalTrials.gov ↗

Amendment history

2026-09-03
Recruiting→Suspended Study Status, Contacts/Locations v4
Recruitment suspended: Lack or research support at the current moment to recruit participants
Trial statusRecruiting→Suspended
Study sitesdetails revised at 1 of 1 site
2025-03-11
Study Status v3
Primary completion date2023-12-30→2026-12-30
Completion date2023-12-30→2026-12-30
2023-06-30
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Study sitesdetails revised at 1 of 1 site
2022-08-19
Study Status, Study Description, Arms and Interventions, Outcome Measures v1
Primary endpoints8 entries, revised
International Prostate Symptom Score (IPSS) ReductionChange Post Void Residual (PVR) ReductionChange Uroflowmetry ImprovementChange
Study description+80 characters
This study is being done to improve the availability of telehealth urology visits. In this study, weinvestigators will compare the usefulness of data collected by three home [...] l visit for lower urinary tract symptoms (LUTS), related to theirprostatic prostateenlargement, compared to an in-person visit. The three devices being in [...] the effectiveness and accuracy of these devices compared to our standard clinical practices and demonstrate theirthe ability of these devices to provide useful information in the home setting. The stud [...] or in office visits. If randomized to the telehealth group, theythe pati [...] [...]
2022-08-17
Original filing
This study is being done to compare usefulness of data collected in uroflowmetry, a test that measures the amount of urine released from the body, at home versus in the doctor's office. Additionally, investigators are assessing patient satisfaction when completing a virtual visit for lower urinary tract symptoms (LUTS), related to prostatic enlargement, compared to an in person visit. The three devices being investigated have not been used in the home setting to make urinary measurements as is typically done in clinic. The goal is to test the effectiveness and accuracy of these devices compared to our standard clinical practices and demonstrate their ability to provide useful information in the home setting.
Trial Details
NCT Number NCT05508165
Lead Sponsor Indiana University
Conditions Urologic Diseases
Enrollment 60 participants
Start Date 2022-08-30
Primary Completion 2026-12-30 (estimated)
Study Completion 2026-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-09-08