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Vaginal Changes After CO2 Laser

University of California, Irvine · with Alma Lasers, National Institute for Biomedical Imaging and Bioengineering (NIBIB) · NCT06691178

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
50
US sites recruiting
1
Study start
May 1, 2023
Record last updated
February 18, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Optical coherence tomography (OCT)

Conditions: Genitourinary Syndrome of Menopause

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • 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
  • Diagnosed as postmenopausal (either by surgical removal of ovaries or natural progression defined as no periods in 1 year)

Exclusion Criteria

  • 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

Recruiting US locations

  • Beckman Laser Institute

    Irvine, CA 92612

    Site contact: Nicole Wakida · 949.824.3295 · nwakida@uci.edu

Study contacts (from the official record)

  • Karla LORENTE, MD · 714-798-9044 · klorente@hs.uci.edu
  • Nicole Wakida · 949.824.3295 · nwakida@hs.uci.edu
Vaginal Changes After CO2 Laser (NCT06691178) | Bored Studies