A study to determine the effect of Intrathecal Morphine in patients on Patient Controlled Analgesia (PCA) Pump with morphine for Postoperative Pain Relief after elective Laparotomy.
Not Applicable
- Conditions
- Health Condition 1: K631- Perforation of intestine (nontraumatic)
- Registration Number
- CTRI/2018/08/015183
- Lead Sponsor
- SRM MEDICAL COLLEGE HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Elective laparotomy.
Patients assessed under ASA I & II
Exclusion Criteria
Patients who have contraindication for subarachnoid block.
Patients who are unable to use a PCA pump.
Patients with a history of drug abuse or allergy to the study drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare total morphine consumption, patient satisfaction and visual analog scale scores.Timepoint: 48 hours
- Secondary Outcome Measures
Name Time Method Comparison of related adverse reactions like nausea, pruritis, sedation, respiratory depressionTimepoint: 48 hours