To compare the degree of patient comfort during propofol injection using dexmedetomidine and dexmedetomidine with lignocaine injection.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064715
- Lead Sponsor
- shri bhausaheb hire government medical college dhule
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
PATIENTS WILLING TO PARTICIPATE IN STUDY
Exclusion Criteria
PATIENT NOT WILLING TO PARICIPATE IN STUDY
PATIENT WITH LIVER DISEASE
PATIENT WITH HISTORY OF OPIOID DEPENDENCE
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO COMPARE THE EFFECTIVENESS OF DEXMEDETOMIDINE AND DEXMEDETOMIDINE-LIGNOCAINE COMBINATION IN PREVENTING PAIN ON PROPOFOL INJECTION.Timepoint: 8 WEEKS
- Secondary Outcome Measures
Name Time Method TO ASSESS THE EFFECTIVENESS OF STUDY DRUGS IN SUPPRESSION OF PRESSOR RESPONSE DURING LARYNGOSCOPYTimepoint: 8 WEEKS