Laser boosts clitoral sensitivity in women, trial finds
NCT ID NCT07152704
First seen Jun 26, 2026 ยท Last updated Jun 26, 2026
Summary
This trial tested a non-ablative Er:YAG laser to improve clitoral sensitivity in 133 adult women who reported decreased sensitivity. Participants received three treatments over 60 days. Two months after the last session, many reported less bothersome symptoms and high satisfaction, with few side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- non-ablative Er:YAG laser
- What this could lead to
- If it works, this could offer a non-invasive option for women with decreased clitoral sensitivity, improving sexual response and satisfaction.
- What could go wrong
- This is a small, completed trial without a control group, so results may not apply to everyone. Long-term effects and safety beyond 2 months are unknown.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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133 people
The number who actually took part.
- Started
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Mar 2022
- Finished
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Dec 2022
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * above 18 years * sexually active at least once per month Exclusion Criteria: * anorgasmia * pregnancy * urinary tract infections * genital infectious diseases of other etiology (HPV, molluscum contagiosum, syphilis, HIV, etc.) * genital bleeding * collagenopathies * ongoing chemotherapy * active genital cancer * patients undergoing pelvic radiotherapy * any genital or extragenital pathology that may interfere with treatment * patients who have limitations in performing a follow-up to this study * patients with psychiatric disorders that may be difficult to treat * patients who have a contraindication to vaginal laser treatments
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Uroclinica
Mendoza, Argentina