Post Operative Pain Clinical Trial
Official title:
Effect of Preoperative Information About Pain on Postoperative Pain Experience and Patient Satisfaction in Adult Elective Orthopedic Patients: A Randomized Controlled Trial
Patients are randomized into 2 groups. The intervention group which receives preoperative
counseling about pain and a control group which does not receive this counseling.
The patients are followed up looking at pain scores and pain experience and satisfaction
with pain management for 2 days post operative.
- All patients admitted for elective upper and lower limb surgery, will be expected to
have a preoperative visit by the anesthetic provider on the day before surgery.
- Those who will have consented to participate in the study will be randomized to either
the intervention or control group.
- The intervention group will receive specific preoperative information about pain in
private by the principal investigator in addition to the preoperative assessment.
- The following variables will be recorded preoperatively: socio-demographics (age,
gender, tribe, education level) and vital signs (pulse rate, blood pressure and oxygen
saturation).
- A Numerical pain score will be explained to patient before it is recorded
preoperatively.
- The patient will also be informed that the pain scores will be repeated after surgery
at (someone will take the pain scores again after surgery at) 0, 6, 12, 24, 48hours or
till discharge if less than 48hours. In addition the pulse rate, number of analgesic
intravenous/ intramuscular injections or tablets needed/or given will be recorded.
- Assessed pain will be classified as no pain (1-3), pain (4-10) but also as no pain (0),
mild (1-3), moderate (4-6) and severe pain (7-10).
- Intra operatively, the anaesthetic technique (general or regional), medications given,
duration of surgery will be recorded in) the questionnaires.
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