Vaginal Changes After CO2 Laser

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of California, Irvine

About this trial

Genitourinary syndrome of menopause (GSM) occurs due to a decline in estrogen levels as a woman approaches menopause. The syndrome negatively impacts women's quality of life and is characterized by vaginal dryness, burning, diminished lubrication, painful intercourse and urinary symptoms such as frequency and urgency. GSM is diagnosed by symptom assessment and physical exam, with current mainstay of treatment being vaginal estrogen. Women with a history of breast cancer, gynecologic cancer, or venous thromboembolism may not be candidates for hormonal therapy. Thus, there has been a quest for effective non-hormonal forms of treatment for GSM. The use of vaginal CO2 laser treatment for GSM has shown promising results.

In this study, we aim to use long-wavelength optical coherence tomography/angiography/elastography (OCT/OCTA/OCE) to document changes that occur in the vaginal epithelium during menopause as well as after treatment for GSM. OCT is a well-studied technology and is widely used in Dermatology and Ophthalmology. In collaboration with the Beckman Laser Institute (BLI), we have developed a non-invasive vaginal probe (HS# 2017-3686). The probe has subsequently been used in previous studies to validate measurements in the vaginal epithelium (HS# 2019-5446). A previous RCT compared clinical response to laser therapy to a control group that received a low level of laser therapy. The study also did not examine histology. This will be a randomized controlled trial in which women will be enrolled into one group receiving laser therapy and compared to a true sham group that will not receive laser therapy at all. Response will be measured primarily by OCT device as well as optional vaginal biopsies. There will also be questionnaires and exam of the vaginal tissue using the VHI.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Birth sex: female

Desire for vaginal laser therapy for GSM

Age >=18 years old

Willingness to forego other treatments for GSM within the study period

Disqualifiers

History of pelvic radiation

On hormone replacement therapy in the prior 3 months

Not able or willing to follow study instructions

Current diagnosis of recurrent UTIs

Trial design

Design model

Parallel

Treatments tested in this trial

  • Optical coherence tomography (OCT)

    Diagnostic test

    The OCT device with cover will be used to take measurements at four areas in the vaginal canal: the proximal posterior aspect, proximal anterior, distal anterior, and distal posterior. The proximal and distal points will be marked on the OCT cover during the first set of measurements. Markings will be used to guide measurements during subsequent visits.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: CO2 Vaginal Laser treatmentExperimental treatment 1 intervention
Group B: Sham - no vaginal laser treatmentSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Vaginal epithelial thickness

OCT measurement of vaginal epithelial thickness

Time frame
Measurements will be obtained once a month for the first three months. Measurements will be obtained at subsequent follow up visits every 3 months for 1 year.
2

Blood vessel density

OCT measurement of blood vessel density

Time frame
Measurements will be obtained once a month for the first three months. Measurements will be obtained at follow up visits every 3 months for 1 year.

Secondary outcomes

1

Vulvovaginal symptoms questionnaire (VSQ)

Validated questionnaire to assess genitourinary syndrome of menopause symptom severity in postmenopausal patients. The score is from 0-20. Higher scores indicate worse symptoms.

Time frame
Questionnaire will be obtained at baseline, during each treatment visit (once a month) and each follow up visit (every 3 months for 1 year).
2

Vaginal health index (VHI)

Scoring system based on provider physical exam assessing optimization of vaginal health. Scores are from 5-25, higher scores indicate better vaginal health.

Time frame
Physical exam will be performed at baseline, during each treatment visit (once a month) and each follow up visit (every 3 months for 1 year).
3

Vaginal Microbiome

Vaginal swab

Time frame
A vaginal swab will be obtained at baseline, during each treatment visit (once a month) and each follow up visit (every 3 months for 1 year).
4

Patient Global Impression

Single item questionnaire assessing subjective improvement on a likert scale.

Time frame
Questionnaire will be completed starting the second treatment visit (once a month) and each follow up visit (every 3 months for 1 year).

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of California, Irvine

Lead sponsor

Alma Lasers

Collaborator

National Institute for Biomedical Imaging and Bioengineering (NIBIB)

Collaborator