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Topical Diclofenac vs. Oral Ibuprofen for Musculoskeletal Pain in Children: A Multi-centre, Randomized Pilot Feasibility Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The TOP-MAP pilot trial has multiple goals. The first goal of this pilot clinical trial is to find out if it will be possible to carry out a study at multiple pediatric emergency department sites (Peds ED) comparing Non-Steroidal Anti-Inflammatory (NSAID) gel applied to a new ankle or knee injury to NSAIDs taken by mouth in kids aged 6-18. The investigators want to determine if the gel works as well or better at reducing pain than NSAIDs given by mouth. Based on studies done on adults, the investigators know that NSAIDs that are applied directly to an injury work as well at relieving pain as NSAIDs that are taken by mouth. Another goal of this pilot trial is to determine if it is possible to recruit participants to the study, and if the participants complete the questionnaire and take the medications as prescribed on Day 1. The participants will be in the study for 14 days. Participants will be required to take the oral NSAID medication and to apply the topical NSAID gel 3 times a day for the first 3 days after their visit to the ED. The investigators will ask the participants to rate their pain on a scale of 0 (no pain) to 10 (worst pain ever) before and after they use the medicine. On day 7, the participants will rate their pain, and their activity level. On day 14 participants will do the same.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Maximum Age: 18
Healthy Volunteers: f
View:

• Age 6 to 18 years old.

• Injury less than or equal to 4 days old

• Non-fractured MSK soft-tissue injury (ankle or knee, confirmed clinically and/or radiographically)

• Pain score of more than or equal to 3 on the verbal numerical rating scale, with movement in the past 2 hours or before analgesia

• Willing and able to complete follow-up surveys as per study protocol

Locations
Other Locations
Canada
Alberta Children's Hospital
RECRUITING
Calgary
Stollery Children's Hospital
NOT_YET_RECRUITING
Edmonton
Contact Information
Primary
Mohamed M Eltorki, MBChB, MSc
mmeltork@ucalgary.ca
403-955-7723
Backup
Angela C Wallace, BA
angela.wallace@ucalgary.ca
403-955-5451
Time Frame
Start Date: 2026-04-02
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 60
Treatments
Experimental: Active topical Diclofenac Diethylamine emulgel
Topical Diclofenac emulgel is a topical NSAID with clinically proven analgesic, anti-inflammatory and antipyretic properties when applied directly to a soft tissue injury. NSAIDs reduce pain principally by inhibiting formation of prostaglandins, leukotrienes and free oxygen radicals. Diclofenac can be expected to produce a direct anti-inflammatory and analgesic effect to the area applied.~Participants randomized to the experimental arm will be given topical diclofenac gel (11.6 mg/g). Dosing is based on the following weight bands:~25 kg: 2 grams/dose;~≥25 kg - \<40 kg: 3 grams/dose; and \>40 kg: 4 grams/dose.
Active_comparator: Active Ibuprofen suspension
Active oral ibuprofen suspension. The ibuprofen suspension dose is 10 mg/kg to a maximum of 600 mg. Ibuprofen is commonly used in ED's as usual care for treatment of soft tissue injuries in pediatric patients.
Related Therapeutic Areas
Sponsors
Collaborators: Hamilton Health Sciences Corporation
Leads: University of Calgary

This content was sourced from clinicaltrials.gov

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