Clinical Trials Directory

Trials / Completed

CompletedNCT02185924

Combination of Continuous Femoral Block and Intravenous Parecoxib For Postoperative Analgesia After Total Knee Arthroplasty

COMBINATION OF CONTINUOUS FEMORAL BLOCK AND INTRAVENOUS PARECOXIB FOR POSTOPERATIVE ANALGESIA AFTER TOTAL KNEE ARTHROPLASTY. A DOUBLE BLIND PROSPECTIVE STUDY.

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Asklepieion Voulas General Hospital · Other Government
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Accepted

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

Conditions

Interventions

TypeNameDescription
DRUGParecoxib
DRUGCONTINUOUS FEMORAL BLOCK WITH ROPIVACAINE 0,2%
DRUGN/S 0.9%

Timeline

Start date
2009-01-01
Primary completion
2011-09-01
Completion
2014-02-01
First posted
2014-07-10
Last updated
2014-07-10

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT02185924. Inclusion in this directory is not an endorsement.