A clinical study to compare two techniques of pain relief(intravenous through blood route vs epidural through a catheter in back) after surgery for cancer treatment using reduction of tumour mass and chemotherapy at high temprature
Not Applicable
Completed
- Conditions
- Health Condition 1: C18- Malignant neoplasm of colonHealth Condition 2: C56- Malignant neoplasm of ovaryHealth Condition 3: C25- Malignant neoplasm of pancreasHealth Condition 4: C20- Malignant neoplasm of rectumHealth Condition 5: C17- Malignant neoplasm of small intestineHealth Condition 6: C16- Malignant neoplasm of stomach
- Registration Number
- CTRI/2020/08/027052
- Lead Sponsor
- Dr BRAIRCH AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1.Posted for CRS and HIPEC surgery.
2.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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate postoperative analgesic efficacy of the analgesic technique.Timepoint: Immediately after extubation, 1 hour, 2 hour, 4 hour, 8 hour, 12 hour, 18 hour and 24 hour.
- Secondary Outcome Measures
Name Time Method To evaluate analgesic requirement intraoperatively.Timepoint: Intraoperatively every 10 minutes requirement of analgesia will be seen and total dose of fentanyl used will be noted.