To compare the effect of two drugs for alleviating propofol injection pain.
Phase 2
- Conditions
- Health Condition 1: null- Physically fit as per ASA guidelines (1&2)
- Registration Number
- CTRI/2017/02/007873
- Lead Sponsor
- INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of AAA physical status 1and 2
Patients between 18-60 years of age of either sex
Patients able to comprehend and willing to participate
Patients in whom propofol is indicated for
Induction of anaesthetia
Exclusion Criteria
Patients refusal to participate
Contraindications to use of palonosetron
Patients with known sensitivity to lignocaine or propofol or palonosetron
Patients on concomitant analgesic or sedative
Patients with presence of infection on the dorsum of the left hand
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method