Effect of site of catheter for bupivacain administration in laparotomy wound on postoperative pai
Not Applicable
- Conditions
- Pain management after laparotomy.
- Registration Number
- IRCT138810142982N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients undergoing midline laparotomy for elective surgeries and sign informed consent for participating in the study
Exclusion Criteria
substance abuse, no appropriate verbal communication, simultaneous other incisions, critically ill or unstable patients, being unconscious or intubated in postoperative period
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total postoperative narcotic consumption. Timepoint: Untill 72 hours based on PCA device. Method of measurement: Patient controlled analgesia device.
- Secondary Outcome Measures
Name Time Method Postoperative nausea and vomitting. Timepoint: daily till 48 hours after surgery. Method of measurement: History taking and clinical records.;Postoperative Cardiavascular complications. Timepoint: daily till 48 hours after surgery. Method of measurement: based on medical reocords.;Postoperative pulmonary complications. Timepoint: daily till 48 hours after surgery. Method of measurement: based on medical reocords.;Wound infection. Timepoint: daily till 5 days after surgery. Method of measurement: Physical examination.;Hospital stay. Timepoint: At the time of discharge. Method of measurement: based on medical reocords.;Postoperative pain. Timepoint: 12 hours intervals for 3 days. Method of measurement: Visual analogue scale.