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Clinical Trial Summary

The intervention will consist of the nursing staff applying 2 grams of diclofenac 1% gel topically to the posterior cervical region four times daily. The control group will receive petroleum jelly topically to the posterior cervical region four times daily. Patients will receive a pre-intervention and post-intervention survey incorporating the Numeric Assessment Scale and Headache Impact Test-6.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05312645
Study type Interventional
Source Loma Linda University
Contact Duc Tran, MD, PhD
Phone 9095589273
Email DATran@llu.edu
Status Recruiting
Phase Phase 3
Start date June 2024
Completion date June 2025

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