Postoperative pain control and satisfactio
Not Applicable
- Conditions
- Acute pain.Acute pain
- Registration Number
- IRCT2013071013948N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
1- patients with non-emergency, elective abdominal surgery who are at least 48 hours after admission. 2- full consciousness 3- aged between 18 and 65 years 4- no history of chronic pain in 5- no history of surgery 6- no history of drug use 7- not having any allergic to painkillers 8- Lack of neurologic disease.
Exclusion criteria:
1- The lack of cooperation during the study, 2 - Discharge or transfer to another section of Surgery 3- Loss of consciousness for any reason.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Satisfaction. Timepoint: Intervention and control groups before and after the intervention. Method of measurement: Questionnaire to assess the level of satisfaction.
- Secondary Outcome Measures
Name Time Method Dose painkiller. Timepoint: 48 hours after surgery. Method of measurement: List the medications used.