Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women
NCT: NCT06925139 · COMPLETED
Brief Summary
This study will test if non-ablative monopolar radiofrequency can help improve vaginal tissue and reduce symptoms of Genitourinary Syndrome of Menopause (GSM) in postmenopausal women. The study is a randomized, sham-controlled clinical trial in which participants and outcome assessors were masked to treatment allocation. The study will examine the impact of the treatment on sexual function, vaginal health, and quality of life over an extended period. There will be two groups in the study: one will receive the non-ablative monopolar radiofrequency treatment, and the other will receive the placebo treatment. Participants will have six treatment sessions and will be checked at the start, end, and three months post-treatment.
Frequently Asked Questions
What is Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women?
Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women is a clinical trial registered under NCT06925139. Current status: COMPLETED.
What is the status of NCT06925139?
The current status of NCT06925139 (Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women) is: COMPLETED.
When did Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women start?
Efficacy of Non-Ablative Radiofrequency on Vaginal and Sexual Health in Postmenopausal Women started on 2024-06-15.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.