Clinical Trials Directory

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UnknownNCT00375362

The Analgesic Effect of Nitroglycerin Patch for Postoperative Pain After Total Knee Replacement

The Analgesic Efficacy of Nitroglycerin Patches for Postoperative Pain in Patients Undergoing Total Knee Arthroplasty

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (planned)
Sponsor
Rabin Medical Center · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

Patients who undergo general anestheesia for total knee arthroplasty pften have sever postoperative pain which hinders their rehabilitation. Nitroglycerin patches have been found to cause alleviation of pain especially when used in conjuction with morphine. Therefore we propose placement of a nitroglycerin patch after total kneee arthroplasty surgery and see how it affects pain scores or causes less nedd for morphine after surgery.

Detailed description

Patients undergoing total knee arthroplasty will be randomized into two groups: control and placebo. Eache patient will undergo total knee arthroplasty under general anesthesia. Both groups will get the same anesthetic protocal. At the end of surgery, before awakening patients will recieve either a nitroglycerin or placebo patch on their back. Both the participant and the investigator will be blinded to the group assisignment. At the end of surgery both groups will recieve morphine for postoperative pain. In the recovery room they will be given patient controlled analgesia with morphine. An investigator blinded to study assisignment will record pain scores, sedation scores, nauseau and vomiting. Patients will be given patient controlled analgesia for 24 hours and they will be followed for pain levels, morphine use, sedation and nauseau levels. The nitroderm or placebo patch will be removed after 24 hours.

Conditions

Interventions

TypeNameDescription
DRUGNitroderm patch

Timeline

Start date
2006-07-01
Completion
2006-09-01
First posted
2006-09-13
Last updated
2006-09-13

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00375362. Inclusion in this directory is not an endorsement.