University of California Davis
Sacramento, California, 95817, United States
NCT Number: NCT02373254
This study is being conducted to evaluate whether NSAIDS are more or less effective in bone healing than opioids in acute fracture pain. Participants will be randomized to one of three groups for first line treatment of pain related to the fracture.
Looking for future studies?
Notify Me18 year–60 year
All sexes
Interventional
Early Phase 1
Sacramento, California, 95817, United States
Pain management in acute fractures is challenging and influenced by several factors contributing to pain perception. These factors include but are not limited to tissue damage by the local impact, mechanical stress at the fracture ends, and central perception of the noxious stimulus. Tissue damage and mechanical stress leads to inflammation and further to local swelling. Swelling itself is significant contributor in pain development.
Ideal pain management would attack pain development at most sites possible. The current clinical practice in the US applies a derivate of an opioid analgesic combined with acetaminophen, thereby influencing pain development at central perception by the opioid analgesic and acetaminophen and a peripheral analgesic effect of acetaminophen. The exact mechanism of the peripheral effect is not known.
This clinical practice disregards the positive effect of medications influencing the peripheral inflammatory response, namely nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs affect pain development by blocking the synthesis of arachidonic acid metabolites, inhibiting peripheral inflammatory response and central pain perception. The major reason for not applying NSAIDs in the treatment of acute fracture pain is an experimental animal study showing decreased bone healing in relation to NSAID usage.
However, clinical data thus far is inconclusive, whether bone healing is affected in humans and whether NSAIDs should be avoided in the setting of bone fractures.
This proposed study will give an answer whether the usage of NSAIDs in acute fractures has a negative effect on bone healing.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ibuprofen 400 mg and 800 mg
Other names: Motrin
Norco 5/325 mg and 10/325 mg
Other names: Norco
Time frame: 12 weeks
fracture healing at 12 weeks followup
Time frame: 1 week, 2 weeks, 6 weeks, 9 weeks and 12 weeks
VAS score
Time frame: 1 weeks, 2 weeks 6 weeks, 9 weeks and 12 weeks
AAOS scale
University of California, Davis
Other
Pain Management With NSAIDS in Acute Ankle Fractures Type Supination, External Rotation (SER) II: A Prospective Randomized, Single Blinded Controlled Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06811090
Ankle Fracture, Ankle Fractures
México, GUSTAVO A MADERO, Mexico
View Trial DetailsNCT06559111
Ankle Fracture, Ankle Fractures
View Trial DetailsNCT02779244
Ankle Fracture, Ankle Fractures
New York, United States
View Trial DetailsNCT00132964
Ankle Fracture, Ankle Fractures
Toronto, Ontario, Canada
View Trial Details