Treatment of Vulvovaginal Laxity by Electroporation: The Jett Plasma Medical for Her II Study

Author:

Fait Tomas12ORCID,Baltazár Tivadar3,Bubenickova Leona4ORCID,Kestranek Jan56,Stepan Martin6,Muller Miroslav7,Turcan Pavel8

Affiliation:

1. Department of Obsterics and Gynaecology, 2nd Faculty of Medicine, Charles University, 150 00 Prague, Czech Republic

2. Department of Health Care Studies, College of Polytechnics Jihlava, 586 01 Jihlava, Czech Republic

3. Department of Agrochemistry, Soil Science, Microbiology and Plant Nutrition, Faculty of AgriSciences, Mendel University in Brno, 613 00 Brno, Czech Republic

4. Faculty of Medicine, Masaryk University, 625 00 Brno, Czech Republic

5. Department of Obsterics and Gynaecology, Hospital Trutnov, 541 01 Trutnov, Czech Republic

6. Department of Obsterics and Gynaecology, Medical Faculty in Hradec Kralove, Charles University, 500 05 Hradec Kralove, Czech Republic

7. Gynedology Pardubice Muller, 530 02 Pardubice, Czech Republic

8. Mediol Centre—Olomouc, 779 00 Olomouc, Czech Republic

Abstract

Introduction: Vaginal laxity is a widespread and undertreated medical condition associated especially with vaginal parity. Aim: To evaluate the efficacy and safety of electroporation therapy treatment of vulvovaginal laxity by the Jett Plasma for Her II device. Methods: The Jett Plasma for Her II Study is a multicentric, prospective, randomized, single-blinded, and controlled study. Women presenting with vaginal laxity were randomized to receive electroporation therapy delivered to the vaginal tissue (active—82 patients) vs. therapy with zero intensity (placebo—9 patients). Results: A total of 91 subjects whose average age was 48.69 ± 10.89 were included. Due to the results of a one-way analysis of variance, it may be concluded that in the case of the vaginal laxity questionnaire (VLQ), there is a statistically significant difference between actively treated patients and the placebo group (F1,574 = 46.91; p < 0.001). In the case of the female sexual function index (FSFI), a one-way ANOVA test also showed a statistically significant difference between the actively treated patients and the placebo group (F1,278 = 7.97; p = 0.005). In the case of the incontinence impact questionnaire-7 (IIQ-7), a one-way ANOVA test showed a statistically significant difference between the actively treated patients and the placebo group (F1,384 = 15.51; p < 0.001). It confirms that improvement of vaginal laxity is conjoined with benefits in symptoms of urinary incontinence. Biopsy performed after the end of the treatment shows an increase in the vaginal mucosa thickness by an average of 100.04% in the active group. The treatment was well tolerated with no adverse events. No topical anesthetics were required. Conclusions: Treatments of vulvovaginal laxity by electroporation therapy achieved significant and sustainable 12-month effectiveness. Responses to the questionnaires also suggest subjective improvement in self-reported sexual function, incontinence, sexual satisfaction, and urogenital distress.

Funder

Educational grant of Compex Ltd., Brno, Czech Republic

Publisher

MDPI AG

Subject

General Medicine

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