drugset / Trial / NCT02684669

Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia During a Burn Injury

NCT02684669

Phase 2 Completed 80 enrolled mads u werner University of Kentucky · collab
RandomizedCrossoverDouble-blindBasic science

Summary

In several rodent studies, it has been demonstrated that very high doses of opioid antagonists (i.e., naloxone 3-10 mg/kg) administered after weeks after recovery from an inflammatory injury may lead to a reinstatement of hyperalgesia and pain behavior. This latent sensitization has recently been demonstrated also to take place in humans. The present study examines if it is possible to foresee individuals who will demonstrate a larger degree of latent sensitization upon challenge with an injury, than others. Using an enriched design high sensitizers (e.g., the upper quartile of individuals developing large areas of secondary hyperalgesia following a mild burn injury) are compared with low sensitizers (lower quartile), regarding the propensity for developing latent sensitization

Timeline

Start
2016-02
Primary completion
2016-09
Completion
2017-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Naloxone Small molecule 3.25 mg/kg Intravenous

Indications

No indication recorded.