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
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | 600mg of Gabapentin will be given orally preoperatively and 200mg for 3 times a day after surgery for 3 days |
| DRUG | Placebo | Placebo 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.