subcutaneous tramadol and methadone in post laparatomy pain control
Phase 2
- Conditions
- pper abdominal laparotomy.Superficial injury of abdomen, lower back, pelvis and external genitals
- Registration Number
- IRCT20120605009948N3
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
• Patients who are electively underwent laparotomy.
• Patients undergoing general anesthesia.
• Patients with no Epidural catheter.
•Do not use analgesic at least 6 hours before surgery
Exclusion Criteria
Pregnancy
Having Diabetes mellitus or chronic renal, liver or heart disease
Previous laparatomy
Opium addiction
Chronic psychological disease
Chronic pain disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain. Timepoint: 1 hours after surgery, 6 hours after surgery, 12 hours after surgery, 18 hours after surgery and 24 hours after surgery. Method of measurement: Using VAS and NPS criteria.
- Secondary Outcome Measures
Name Time Method