At a glance
ClinicalIndex Comparison RecordN/ACompleted· 75 enrolled
Drug / intervention
Fluoroscopyradiation
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.
InterStim Implantation Rates Following Percutaneous Nerve Evaluation With Fluoroscopy Versus Without
In Brief
A clinical study evaluating Fluoroscopy for Overactive Bladder and 2 related conditions. Completed, enrolled 75 participants across 1 site.
Detailed Summary
The investigators propose a randomized control trial comparing the rate of implantation of the InterStim device following Percutaneous Nerve Evaluation (PNE) performed with or without fluoroscopic guidance.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOveractive Bladder, Urinary Incontinence, Fecal Incontinence
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 2016
Enrollment StartApr 2016
Primary CompletionApr 2019
TodayJul 2026
First PostedFeb 9, 2016
Enrollment StartApr 1, 2016
Primary CompletionApr 1, 2019
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 10.4 years ago
Interventions
Fluoroscopyradiation