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Clinical Trial Summary

Combination of continuous femoral block with parEcoxib vs placebo. Investigation of morphine consumption, opioid sparing effects, VAS pain scores, haemodynamics, Anxierty scores, transfusion requirements , Range of motion and rehabilitation parameters between two groups


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)


Related Conditions & MeSH terms

  • POSTOPERATIVE ANALGESIA FOR TKA PARECOXIB/CFB

NCT number NCT02185924
Study type Interventional
Source Asklepieion Voulas General Hospital
Contact
Status Completed
Phase Phase 2/Phase 3
Start date January 2009
Completion date February 2014