DigiVibe Device Study for Pain Reduction

Completed Not Applicable NCT06987201

Study Description

Evaluating the Effectiveness of the DigiVibe Device in Reducing Pain During Injections and Fingersticks

Study Details

Registry ID:
NCT06987201
Conditions:
Healthy
Phase:
Not Applicable
Target Enrollment:
20 participants
Start Date:
Age Range:
18–999 years
Healthy Volunteers:
No

Study Locations (1 site)

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