Bonipar for Acute & Chronic Muskuloskeletal Pain - Clinical Trial

What is the Purpose of this Study?

We are doing this study to learn more about the effectiveness and safety of the study drug (Bonipar), a topical (on the skin) herbal oil extracts agent for treating muscle and skeletal pain.

What is the Condition Being Studied?

Chronic Pain

Who Can Participate in the Study?

Adults (18 years and older) who are not pregnant or expecting to become pregnant who have a single area of pain they would like to treat.

Age Group
Adults

What is Involved?

This study involves 2 visits to Duke University Hospital.

If you choose to join the study, you will:
- Answer questions about your pain
- Be randomly assigned (a fair 50/50 chance) to get the study drug (Bonipar) or diclofenac (an FDA-approved NSAID)
- Have a baseline visit that lasts about 1.5 hours
-Treat a single area of pain morning and night with your assigned solution
-Take home and fill out a study questionnaire and document your study drug process
-Return in 1 week with any leftover study drug and your study diary

Study Details

Full Title
Efficacy of a topical pain relief spray containing herbal oil Extracts (Bonipar) among individuals with acute and chronic musculoskeletal pain
Principal Investigator
Pain Medicine Specialist
Protocol Number
IRB: PRO00081546
NCT: NCT03471507
Phase
Phase II
ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate
Contact the Duke Recruitment Innovation Center
MyResearchPartners@duke.edu
or
919-681-5698