Photobiomodulation for Vaginal Dysfunctions: Home-Based vs Outpatient Treatment

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-75
SponsorPatricia Lordelo

About this trial

Vaginal disorders, including vulvovaginal candidiasis (VVC), bacterial vaginosis (BV), and genitourinary syndrome of menopause (GSM), are highly prevalent conditions that significantly affect women's quality of life and sexual health. These disorders are associated with inflammatory changes, vaginal dysbiosis, and symptoms such as pruritus, abnormal vaginal discharge, dryness, and dyspareunia. In this context, photobiomodulation has emerged as a noninvasive therapeutic approach with anti-inflammatory and tissue-repair properties. This study is a randomized clinical trial designed to compare the therapeutic response to blue LED photobiomodulation (401 ± 5 nm) delivered through home-based and outpatient treatment protocols. A total of 150 women aged 18 to 75 years with a diagnosis of GSM, BV, or VVC will be enrolled and randomly assigned to one of two treatment groups. Clinical and laboratory assessments will be performed before and after treatment. Participants will also complete the Female Sexual Function Index (FSFI) and the 36-Item Short Form Health Survey (SF-36). Outcomes will include the evaluation of gynecological signs and symptoms, sexual function, quality of life, treatment adherence, and adverse events. The anticipated risks are minimal and primarily related to potential discomfort during gynecological examinations and possible embarrassment associated with discussing sensitive health information. The study is expected to demonstrate that photobiomodulation may improve clinical and functional outcomes, representing a safe, non-hormonal therapeutic alternative for the management of vaginal disorders.

Eligibility criteria

Qualifiers

Women aged 18 to 75 years.

Clinical and/or laboratory-confirmed diagnosis of Genitourinary Syndrome of - Menopause (GSM), Bacterial Vaginosis (BV), or Vulvovaginal Candidiasis (VVC), according to established diagnostic criteria.

Ability to understand study procedures and provide written informed consent.

Willingness to comply with study procedures and follow-up assessments.

Disqualifiers

Pregnancy.

Use of a pacemaker or other implanted electronic medical device.

Active gynecological malignancy or suspicion of gynecological cancer.

Neurological and/or psychiatric disorders associated with cognitive impairment that may interfere with understanding study procedures.

Trial design

Treatments tested in this trial

  • Blue LED Photobiomodulation

Treatment groups

150 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Sponsors and collaborators

Patricia Lordelo

Lead sponsor

Centro de Atenção ao Assoalho Pélvico

Sponsor institution

Escola Bahiana de Medicina e Saude Publica

Collaborator