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NCT03595215 · ClinicalTrials.gov registry record · NA
Posterior Tibial Nerve Stimulation's Effectiveness in UI Frequency in Overactive Patients in Home
A NA study, sponsored by Theranova, L.L.C..
- Completed
- Registry status
- NA
- Development phase
- 18
- Enrollment target
NCT03595215: Completed NA study, sponsored by Theranova, L.L.C..
NCT03595215 is a NA study that has completed, run by Theranova, L.L.C.. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03595215, a NA study, has completed, sponsored by Theranova, L.L.C..
- COMPLETED
- Registry status
- NA
- Development phase
- 18 participants
- Enrollment target
Study Summary
This pilot clinical study, which focuses on feasibility and proof-of-principle, will be conducted in 11 female subjects (55-100 years old) with UI. Subjects will use the device three times a week for 8 weeks and complete 3-day "voiding diaries" to record instances of UI episodes and OAB quality of life.
Interventions
- DEVICE TENS
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2018-09-10 |
| Est. Completion | 2019-09-17 |
| Phase | NA |
What the finished NCT03595215 record still lists
NCT03595215 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which TENS is the first listed.
NCT03595215 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03595215 about?
NCT03595215 is a clinical study titled "Posterior Tibial Nerve Stimulation's Effectiveness in UI Frequency in Overactive Patients in Home". This pilot clinical study, which focuses on feasibility and proof-of-principle, will be conducted in 11 female subjects (55-100 years old) with UI. Subjects will use the device three times a week for 8 weeks and complete 3-day "voiding diaries" to record instances of UI episodes and OAB quality of l...
What is the current status of trial NCT03595215?
This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2018-09-10. Estimated completion is 2019-09-17.
What interventions are being tested in trial NCT03595215?
The interventions under investigation include: TENS (DEVICE).
Who is sponsoring clinical trial NCT03595215?
This trial is sponsored by Theranova, L.L.C., which has 11 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03595215's enrollment target sits among peer trials
18 1863rd of 2000 higher than 130 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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