Pain management is becoming an important ethical responsibility of the medical profession and a focus of the health care system. However, there are limited literature evaluate the postoperative pain experience and management in our local setting.
- Study Type: Observational [Patient Registry]
- Study Design
- Time Perspective: Cross-Sectional
- Study Primary Completion Date: September 2014
We need to identify those patients who, from a demographic, psychology and surgical viewpoint, are more at risk of experiencing postoperative pain.
- Procedure: operation
Arms, Groups and Cohorts
- postoperative pain
Clinical Trial Outcome Measures
- postoperative pain experience
- Time Frame: 2 weeks
- To determine patient’s postoperative pain experience during and 2 weeks after discharge from hospital.
Participating in This Clinical Trial
- 1. Adult with age ≥ 18 who undergo operation
- 1. Refused to give informed consent
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- University of Malaya
- Provider of Information About this Clinical Study
- Overall Official(s)
- Wang Chew Yin, Principal Investigator, University Malaya
- Overall Contact(s)
- Prof Wang Chew Yin, 03-79492052, email@example.com
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