Comparison between two pain reducing technique after operatio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- With diagnosis of abdominal malignancy
- Registration Number
- CTRI/2017/07/008987
- Lead Sponsor
- AIIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age of 18 years or older, but less than 70 years.
2.Clinical diagnosis of primary abdominal malignancy.
3.Agree to receive postoperative patient-controlled analgesia.
4.Agree to participate in the study and have signed written informed consent.
Exclusion Criteria
1.Complicated with mental illness, severe heart disease (NYHA classification 3), any renal or hepatic disorder before surgery.
2.Contraindications of epidural anesthesia.
3.Allergic to any drug used during the study.
4.Patients who are likely to be electively ventilated in postoperative period.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rescue analgesia in post operative periodTimepoint: Rescue analgesia in post operative period
- Secondary Outcome Measures
Name Time Method Post operative pain scoreTimepoint: 1,2,4,8,12,18,24 hrs post operative period.