Comparison of pain relief in the postoperative period with Continuous epidural infusion and Patient controlled epidural device for patients undergoing major abdominal oncologic surgeries
Not Applicable
- Conditions
- Health Condition 1: C189- Malignant neoplasm of colon, unspecifiedHealth Condition 2: C259- Malignant neoplasm of pancreas, unspecifiedHealth Condition 3: C19- Malignant neoplasm of rectosigmoidjunctionHealth Condition 4: C20- Malignant neoplasm of rectumHealth Condition 5: C569- Malignant neoplasm of unspecifiedovaryHealth Condition 6: C55- Malignant neoplasm of uterus, partunspecified
- Registration Number
- CTRI/2020/01/022973
- Lead Sponsor
- St Johns Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients above age of 18 years to 59 years belonging to ASA I, II, III undergoing major abdominal oncologic surgery in St. Johnâ??s Medical College Hospital during the study period.
Exclusion Criteria
Patients who have a clinical or laboratory contraindication to the placement of an epidural catheter like bleeding diathesis, severe hypovolemia, elevated intracranial pressure (particularly with an intracranial mass), severe aortic stenosis, severe mitral stenosis and infection at the site of injection.
Inability to use the PCEA device
Patient posted for Gastrectomy.
Patients who have a known allergy to the local anaesthetic or opioid used
Patient refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method