Can a simple cooling spray ease pain during gynecologic exams?
NCT ID NCT06227052
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a cooling spray (vapocoolant) applied to the cervix before a numbing injection can reduce pain during gynecologic procedures. 98 adults participated, receiving either the spray or a placebo. The goal was to see if this simple, drug-free approach improves comfort and satisfaction.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Num vapocoolant spray (a cooling spray applied to the cervix)
- What this could lead to
- If it works, this could offer a simple, drug-free way to reduce pain during common gynecologic procedures.
- What could go wrong
- This is a small, completed Phase 4 trial. The spray is already FDA-approved for skin, but using it on the cervix is new. Results may not apply to all patients or procedures.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
98 people
The number who actually took part.
- Started
-
Feb 2024
- Finished
-
Mar 2025
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * Age 18 years of age or older Undergoing a procedure requiring paracervical block English-speaking Able and willing to sign the informed consent form and agree to terms of the study Exclusion Criteria: * Required or requested narcotics, anxiolytics, IV sedation, or general anesthesia for the procedure Declines or has a contraindication/allergy to ibuprofen Previously received vapocoolant spray in a medical setting Contraindications or allergies to lidocaine for paracervical block or vapocoolant spray components (1,1,3,3-pentafluoropropaine or 1,1,1,2-tetrafluroethane)
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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
-
Queens Medical Center POB1 Clinic 1004
Honolulu, Hawaii, 96813, United States
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