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Clinical Trials in Canada / NCT06966206
Recruiting Phase 3

Multiprofen-CC to Reduce Pain in Hand Arthritis

NCT06966206 · tracked via the Priya Life Science Canada tracker
Phase
Phase 3
Started
2026-03-09
Last updated
2026-05-04

Condition(s) studied

Hand Osteoarthritis

Investigational drug(s) / intervention(s)

Multiprofen-CC™ plus standard treatmentPlacebo plus standard treatment

Multiprofen-CC™ plus standard treatment: Standard care pain medications and topical Multiprofen-CC™ (1g TID) for 2 weeks

Placebo plus standard treatment: Standard care pain medications and visually identical topical placebo (1g TID) for 2 weeks

Study summary

This clinical trial aims to find out if using 1 gram of Multiprofen-CC cream on the hands three times a day for 4 weeks can help reduce pain in adults with hand osteoarthritis, compared to a placebo (a cream with no active medicine). The research team will also look at how Multiprofen-CC affects hand function, opioid use, and how patients feel about their overall improvement. In addition, the research team will keep track of any side effects.

Participants will:

* Use both Multiprofen-CC and a placebo (a cream with no active medicine) during the study, in a random order.
* Be asked to apply 1 gram of cream to their hands three times a day for 2 weeks, following the manufacturer's instructions.
* Attend a visit before starting the study, after 2 weeks, and after 6 weeks.
* Report any symptoms they experience during the study.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (18+) * Have been diagnosed with hand osteoarthritis according to American College of Rheumatology criteria * Experience pain and/or loss of function in one or both hands that interferes with daily life * Provide informed consent Exclusion Criteria: * Unable to consent * Unable or unwilling to follow study protocol * Known allergy or contraindication to any of the study drugs or their ingredients * Have open wounds/cuts and/or skin conditions on the hand area * Pregnant or breastfeeding * History of impaired kidney or liver function * Rheumatoid or other inflammatory arthropathy * Hand surgery within the past 6 months or planned within the study period. * Use daily opioids (other than short acting codeine) for a chronic pain condition other than hand arthritis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
St. Joseph's Healthcare Hamilton Hamilton Ontario Recruiting

More St. Joseph's Healthcare Hamilton trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06966206 on ClinicalTrials.gov ↗ ← All trials in Canada