Clinical Trials Directory

Trials / Completed

CompletedNCT01307202

Morphine Consumption in Joint Replacement Patients, With or Without Gabapentin Treatment

Multiple Doses of Gabapentin and Postoperative Morphine Consumption in Total Knee Arthroplasty

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
101 (actual)
Sponsor
McMaster University · Academic / Other
Sex
All
Age
19 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Total knee arthroplasty is amongst the most painful procedures postoperatively, and pain management can be a challenge. Different measures have been introduced to manage severe postoperative pain int hese patients. Previous studies have investigated gabapentin in acute postoperative pain and demonstrated reducted pain, postoperative morphine consumption, morphine related side effects, and postoperative pain scores. To date, this analgesia adjunct has yet to be investigated in total joint arthroplasty patients.

Detailed description

The study was submitted to Health Canada and received the letter of no objection. A randomized, double-blind, placebo-controlled study. The randomization scheme will be prepared and will be done by the pharmacy department at McMaster University. Ninety patients undergoing primary knee arthroplasty will be recruited from the preoperative clinic. Forty-five patients in each population will be allocated to a gabapentin group and the other forty-five to a placebo group.

Conditions

Interventions

TypeNameDescription
DRUGGabapentin600mg of Gabapentin will be given orally preoperatively and 200mg for 3 times a day after surgery for 3 days
DRUGPlaceboPlacebo will match the the gabapentin pill and will be given orally.

Timeline

Start date
2007-10-01
Primary completion
2011-02-01
Completion
2011-02-01
First posted
2011-03-02
Last updated
2014-11-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01307202. Inclusion in this directory is not an endorsement.