Actively Recruiting

Phase Not Applicable
Age: 14Years +
FEMALE
Healthy Volunteers
NCT06933381

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

Age: 14Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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