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Spots Global Cancer Trial Database for Sphenopalatine Ganglion Block for Headache After Concussion

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Trial Identification

Brief Title: Sphenopalatine Ganglion Block for Headache After Concussion

Official Title: A Phase II Randomized Controlled Double-Blind Clinical Trial of Sphenopalatine Ganglion (SPG) Block for Headache After Concussion

Study ID: NCT04650282

Study Description

Brief Summary: This clinical trial will enroll participants to evaluate the effects of SPG block on post-traumatic headache. The study hypothesizes that patients that receive a SPG block with lidocaine vs. placebo (saline) will have a lower number of headache days in the week following the procedure, and will also report lower symptom scores. Eligible participants will receive one treatment (SPG block) as well as complete surveys prior to and after receiving treatment (for a total of approximately 2 weeks).

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Michigan, Ann Arbor, Michigan, United States

Contact Details

Name: Michael Popovich, MD

Affiliation: University of Michigan

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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