drugset / Trial / NCT02344264

Effect of Nervus Cutaneous Femoris Lateralis-Blockade on Moderate Pain Responders After Total Hip Arthroplasty

NCT02344264 ↗

Phase 4 Completed 60 enrolled Daniel Hägi-Pedersen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The patients will be included the 1. or 2. day after surgery. All THA patients will be screened. Those reporting VAS \> 40 during active 30 degrees hip flexion will be asked to participate. Included patients will receive 2xNCFL (singleshot) first placebo (8 ml saline) and then ropivacaine (8 ml ropivacaine 7,5mg/ml) or the other way around (randomized). There will be 45 minutes between the two blockades. The blockades will be ultrasound guided.

Timeline

Start
2015-01
Primary completion
2015-09
Completion
2015-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 7.5 mg/ml Other
Subject Ropivacaine Other / unclassified 8 ml Other