Randomized clinical trial: non-ablative radiofrequency for dyspareunia in postmenopausal women

This dataset contains de-identified participant data from a randomized, single-blind, sham-controlled clinical trial evaluating the efficacy of non-ablative capacitive–resistive monopolar radiofrequency for the treatment of dyspareunia in postmenopausal women.

The dataset includes baseline, post-treatment, and 12-week follow-up measurements. Primary outcome data correspond to pain intensity during vaginal dilator insertion, measured using a 0–10 numeric rating scale. Secondary outcomes include sexual function assessed with the Female Sexual Function Index (FSFI), vaginal lubrication measured on an 11-point scale, and quality of life assessed using the SF-12 questionnaire.

A data dictionary describing all variables and coding, as well as the statistical analysis code used in the study, are included.

All data have been fully de-identified in accordance with applicable ethical and data protection standards. Access to the dataset is restricted and available upon reasonable request to the corresponding author, subject to ethical approval and data use agreement.