Trials / Completed
CompletedNCT04201041
Pudendal Nerve Fluoroscopic Guided Pulsed Radiofrequency for Treatment of Superficial Dyspareunia
Trans-gluteal Versus Trans-vaginal Pudendal Nerve Fluoroscopic Guided Pulsed Radiofrequency for Treatment of Superficial Dyspareunia: a Prospective Cohort Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- South Egypt Cancer Institute · Academic / Other
- Sex
- All
- Age
- 16 Years – 46 Years
- Healthy volunteers
- Not accepted
Summary
Superficial dyspareunia represents a major health problem especially for the newly wed couples. Pulsed radiofrequency for pudendal nerve is a non-neurolytic neuromodulatory method that is effective in relief of this type of pain. Objectives: to evaluate the efficacy of bilateral pudendal nerve fluoroscopic guided pulsed radiofrequency in treatment of intractable non-organic dyspareunia, and compare between trans-gluteal and transvaginal approaches regarding patient comfort and satisfaction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | pudendal nerve pulsed radiofrequency | received pudendal nerve pulsed radiofrequency through trans-vaginal approach or trans-gluteal approach |
Timeline
- Start date
- 2018-12-01
- Primary completion
- 2020-03-20
- Completion
- 2020-03-25
- First posted
- 2019-12-16
- Last updated
- 2020-04-09
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04201041. Inclusion in this directory is not an endorsement.