Vapocoolant Spray to Reduce Pain With Nexplanon Insertion
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Reducing Pain With Nexplanon Implant Insertion
In brief
The purpose of this study is to assess if Pain Ease vapocoolant spray decreases pain associated with lidocaine injection during Nexplanon insertion procedures.
Key facts
- Study ID
- NCT06933381
- Run by
- Queen's Medical Center
- People needed
- 70
- Starts
- 2025-06-16
- Expected to finish
- 2026-05-01
- Last updated by the study team
- 2026-01-09
Who can join
Age: 14 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- At least 14 years or older
- Undergoing an etonogestrel implant insertion in the arm in POB1 Suite 1004 or POB2 Suite 402
- English speaking
- Able and willing to sign the informed consent form and agree to terms of the study
You may not qualify if…
- Required or requested narcotics, anxiolytics, IV sedation, or general anesthesia for the procedure
- Known previous exposure to vapocoolant spray
- Nexplanon removal and reinsertion same day during visit in the same arm
- Contraindications to vapocoolant spray components (ethyl chloride and 1,1,1,3,3-pentafluoropropane/1,1,1,2-tetrafluroethane)
- Unable to provide written, informed consent in English
Where it is running
- Queens Medical Center POB 2 Suite 402 — Honolulu, Hawaii, United States (enrolling)
- Queens Medical Center POB1 Clinic 1004 — Honolulu, Hawaii, United States (enrolling)
- Women's Center Queen's North Hawai'i Community Hospital Suite #124 and #120 — Waimea, Hawaii, United States
Full record on ClinicalTrials.gov
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