Recruiting

CO2 Laser Therapy

Sponsor:

UCLA

Code:

NCT06691178

Conditions

Genitourinary Syndrome of Menopause

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Interventions

Optical coherence tomography (OCT)

Study Details

Brief summary:

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.

Conditions

Genitourinary Syndrome of Menopause

Study ID

NCT06691178

Start date

May 1, 2023

Status verified date

Feb, 2026

Completion date

Jul 1, 2027

Anticipated

Primary completion date

May 1, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Birth sex: female
2. Desire for vaginal laser therapy for GSM
3. Age >=18 years old
4. Willingness to forego other treatments for GSM within the study period
5. Diagnosed as postmenopausal (either by surgical removal of ovaries or natural progression defined as no periods in 1 year)

Exclusion Criteria:

1. History of pelvic radiation
2. On hormone replacement therapy in the prior 3 months
3. Not able or willing to follow study instructions
4. Current diagnosis of recurrent UTIs

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: CO2 Vaginal Laser treatment

Laser treatment with a Fractional/Pixel CO2 laser (Femilift, Alma Lasers) will be performed with the following settings and procedure: single pulse; first pass 50-100 millijoules/pixel of energy, and 50-100 millijoules/pixel for the second pass. The energy level will be adjusted within the range based on the subject's comfort level. The same procedures will be followed for the sham group but no pulse will be generated.

sham comparator: Sham - no vaginal laser treatment

The vaginal laser probe will be placed as usual but no energy will be delivered to the tissue.

Interventions

Optical coherence tomography (OCT)

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.

Primary outcome measure

  • 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. ]
  • 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. ]

Central Contacts and Locations

Central contacts

Locations

Beckman Laser Institute

Recruiting

Irvine, California, United States, 92612

Contacts

Principal Investigator:

Felicia Lane, MD

More Information

Sponsor

University of California, Irvine

Last update posted

Feb 18, 2026

Last verified

Feb, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, Irvine on 2026-02-18.