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NCT04122703 · ClinicalTrials.gov registry record · NA
Trial of Tibial Nerve Stimulation for Treating Sexual Dysfunction
A NA study of Female Sexual Dysfunction, sponsored by Stony Brook University.
- Completed
- Registry status
- NA
- Development phase
- 66
- Enrollment target
- 1
- Study location
NCT04122703: Completed NA study of Female Sexual Dysfunction, sponsored by Stony Brook University.
NCT04122703 is a NA study of Female Sexual Dysfunction that has completed, run by Stony Brook University. The registered enrollment target is 66 participants, below the 73-participant average among 4 other Female Sexual Dysfunction trials with a reported enrollment target (10% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04122703, a NA study of Female Sexual Dysfunction, has completed, sponsored by Stony Brook University.
- COMPLETED
- Registry status
- NA
- Development phase
- 66 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to understand the efficacy of PTNS versus a placebo in the treatment of female sexual dysfunction syndrome.
Primary Outcome
Female Sexual Function Index (FSFI) is a 19-item questionnaire used to assess female sexual function. Minimum score is 1.2 and maximum score is 36. A score of 26.55 or lower is classified as sexual dysfunction
Conditions Studied
Interventions
- DEVICE percutaneous tibial nerve stimulation (PTNS)
- DEVICE Sham procedure
Study Locations (1)
New York
- Stony Brook Medicine Women's Pelvic Health And Continence Center - Stony Brook
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2019-09-15 |
| Est. Completion | 2023-06-30 |
| Phase | NA |
What the finished NCT04122703 record still lists
NCT04122703 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 73-participant average among 4 other Female Sexual Dysfunction trials with a reported enrollment target (10% lower).
The record links to 1 condition, with Female Sexual Dysfunction appearing as the primary indexed condition, and to 2 interventions - of which percutaneous tibial nerve stimulation (PTNS) is the first listed.
NCT04122703 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT04122703 about?
NCT04122703 is a clinical study titled "Trial of Tibial Nerve Stimulation for Treating Sexual Dysfunction". The purpose of this study is to understand the efficacy of PTNS versus a placebo in the treatment of female sexual dysfunction syndrome.
What is the current status of trial NCT04122703?
This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2019-09-15. Estimated completion is 2023-06-30.
What conditions does trial NCT04122703 study?
This clinical trial studies the following conditions: Female Sexual Dysfunction.
What interventions are being tested in trial NCT04122703?
The interventions under investigation include: percutaneous tibial nerve stimulation (PTNS) (DEVICE), Sham procedure (DEVICE).
Who is sponsoring clinical trial NCT04122703?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04122703 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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