Effectiveness of Radiofrequency Combined With Ultrasound for the Treatment of Postpartum Dyspareunia
Recruiting
N/A
Interventional Study
Dyspareunia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 34 (estimated)
- Sponsor
- Institut Investigacio Sanitaria Pere Virgili · Other
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About This Trial
The objective of this community-based, non-randomized, quasi-experimental study is to assess the effectiveness of BTL EXILIS technology-based on combined radiofrequency and ultrasound-in women of childbearing age from an industrialized country with a diagnosis of dyspareunia following vaginal delivery.
The primary research question is:
\- Do patients experience a resolution of pain during sexual…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women of childbearing age
* Medical history of at least one prior vaginal delivery
* Reported persistent pain during penetrative sexual intercourse
* Meeting the clinical criteria for dyspareunia
* Moderate to severe pain level, defined as a score of 4 or higher on the Visual …
Contacts