A clinical study comparing two routes for giving two classes of drugs by comparing postoperative quality of recovery using a 15 point questionnaire after cancer surgeries of abdomen under general anaesthesia.
- Conditions
- Health Condition 1: C179- Malignant neoplasm of small intestine, unspecifiedHealth Condition 2: C55- Malignant neoplasm of uterus, partunspecified
- Registration Number
- CTRI/2024/07/070242
- Lead Sponsor
- Arpita Thombre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Known gastrointestinal or genitourinary cancer patients
ASA grade III-IV
Patients undergoing oncological abdominal surgeries under general anaesthesia
1) Patient refusal 2) BMI = 30 kg/m 2
3) Clinically significant neurologic, psychiatric, CVS 4) Critically ill patient
renal, respiratory and hepatic disease
5) Coagulation abnormalities 6) Local infection (for epidural)
7) Allergy to study drugs, pregnancy, drug abuse/ 8) Those who received analgesic, anxiolytic, antipschyciatric substance abuse medication within 6 hours before surgery
9) Redo surgery
10)Failure of extubation within 6 hours of surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method