Total Knee Arthroplasty
Conditions
Keywords
nitroglycerin, morphine, patient controlled analgesia, total knee arthroplasty
Brief 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.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Healthy patients undergoing total knee arthroplasty
Exclusion criteria
* Pshychiatric disorder * Allergy to nitroglycerin or morphine * Chronic renal failure * Migraine headaches * Hypotension
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain scores | — |
| morphine use | — |
| sedation score | — |
| nausea and vomiting | — |
Countries
Israel