Health Condition 1: null- With diagnosis of abdominal malignancy
Conditions
Interventions
Intervention1: Group IV: IV lignocaine and fentanyl infusion
Control Intervention1: Group EPI: Epidural Ropivacaine and fentanyl infusion
Sponsors
AIIMS
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rescue analgesia in post operative periodTimepoint: Rescue analgesia in post operative period | — |
Secondary
| Measure | Time frame |
|---|---|
| Post operative pain scoreTimepoint: 1,2,4,8,12,18,24 hrs post operative period. | — |
Countries
India
Contacts
Public ContactDr Rudranil Nandi
All India Institute of Medical Sciences
Outcome results
None listed