Actively Recruiting
Vapocoolant Spray to Reduce Pain With Nexplanon Insertion
Led by Queen's Medical Center · Updated on 2026-01-09
70
Participants Needed
3
Research Sites
45 weeks
Total Duration
On this page
Sponsors
Q
Queen's Medical Center
Lead Sponsor
L
Lakshmi Devi and Devraj Sharma Endowment
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to assess if Pain Ease vapocoolant spray decreases pain associated with lidocaine injection during Nexplanon insertion procedures.
CONDITIONS
Official Title
Vapocoolant Spray to Reduce Pain With Nexplanon Insertion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Queens Medical Center POB 2 Suite 402
Honolulu, Hawaii, United States, 96813
Actively Recruiting
2
Queens Medical Center POB1 Clinic 1004
Honolulu, Hawaii, United States, 96813
Actively Recruiting
3
Women's Center Queen's North Hawai'i Community Hospital Suite #124 and #120
Waimea, Hawaii, United States, 96743
Not Yet Recruiting
Research Team
S
Sarah Murayama, MD
CONTACT
M
Mary Tschann, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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