efficacy of fentanyl and neostigmine combination in spinal anaesthesia
Not Applicable
- Registration Number
- CTRI/2022/06/043043
- Lead Sponsor
- hitender kumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
asa 1 and 2, surferies below the umbilicus under spinal anaesthesia
Exclusion Criteria
platelet count less than 100000/cu mm
asa class 3 and 4
sensitivity to local anaesthestics
history of heart failure or kidney or liver disease
history of neurological disorder
failed spinal anaesthesia
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method onset of sensory, motor blockade and mximum dermatome achieved, time for 2 segment regression of sensory blockadeTimepoint: 6 months
- Secondary Outcome Measures
Name Time Method haemodynamic parameter- HR, SBP, DBP, MBP, SPO2..incidence of sedation/nausea vomiting upto 2 hours postoperativelyTimepoint: 2 hours postoperatively