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NCT01525485 · ClinicalTrials.gov registry record
Vaginal Electrical Stimulation Versus Neuromodulation
A clinical trial, sponsored by University of Oklahoma.
- Completed
- Registry status
- 34
- Enrollment target
NCT01525485 is a clinical trial that has completed, run by University of Oklahoma. The registered enrollment target is 34 participants.
The verdict
NCT01525485 has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- 34 participants
- Enrollment target
Study Summary
This prospective study compares quality of life measures of patients with refractory overactive bladder, between two modes of neuromodulation: vaginal electrical stimulation (Group A) and sacral nerve stimulation (Group B). The specific aims are: 1\. To characterize patient symptom bother score, quality of life, and body image scores in patients obtaining sacral nerve stimulation, as compared to vaginal electrical stimulation. \- Hypothesis 1: Both modes of neuromodulation will impact patients' scores in quality of life, patient symptoms, and body image questionnaires.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2011-03 |
| Est. Completion | 2016-04 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01525485
The ClinicalTrials.gov registry entry for NCT01525485 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT01525485 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01525485 about?
NCT01525485 is a clinical study titled "Vaginal Electrical Stimulation Versus Neuromodulation". This prospective study compares quality of life measures of patients with refractory overactive bladder, between two modes of neuromodulation: vaginal electrical stimulation (Group A) and sacral nerve stimulation (Group B). The specific aims are: 1\. To characterize patient symptom bother score, q...
What is the current status of trial NCT01525485?
This trial is currently completed. The enrollment target is 34 participants. The study started on 2011-03. Estimated completion is 2016-04.
Who is sponsoring clinical trial NCT01525485?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
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