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Intravaginal non-Ablative Radiofrequency Treatment ...
Intravaginal non-Ablative Radiofrequency Treatment for Genitourinary Syndrome of Menopause - Patricia Lordelo
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The study aims to investigate the clinical response and adverse effects of intravaginal non-ablative radiofrequency (RF) treatment for genitourinary syndrome of menopause (GSM). The research followed the principles of the Helsinki Declaration and was registered on clinicaltrial.gov. The pilot study included women up to 65 years old with established menopause and symptoms of vulvovaginal atrophy. Participants were excluded if they used pacemakers, hormonal replacement, had metallic prostheses in the pelvic region, or had a vaginal infection. The treatment involved five RF sessions with a seven-day interval between them using a capacitive electrical transfer method. Clinical response criteria were assessed at the beginning and end of each session and at 7 days and one month after the end of treatment. A likert scale was used to measure participant satisfaction with the treatment. Adverse effects were monitored. Eleven women completed the protocol, and after one and three months of treatment, they reported reduced clinical symptoms and were satisfied with the clinical response. No adverse effects were reported. The preliminary result is promising, but larger clinical trials are needed to increase the validity of the study.
Keywords
intravaginal non-ablative radiofrequency treatment
genitourinary syndrome of menopause
clinical response
adverse effects
vulvovaginal atrophy
likert scale
participant satisfaction
reduced clinical symptoms
larger clinical trials
Helsinki Declaration
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