MedPath

Comparison of two local anaesthetics in spinal anaesthesia

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/04/041908
Lead Sponsor
Sree Balaji Medical College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA 1&2

Undergoing infra umbilical surgery under subarachnoid block

Consenting to participate in the study

Exclusion Criteria

Patient refusal

Allergy to local anaesthetics

Local infection at the site of block

Bleeding disorder

Pre operative hypotension

pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
onset and duration of sensory blockTimepoint: The onset of sensory block at T10 will be monitored from positioning the patient after spinal anaesthesia at every 30 seconds and thereafter at every 3 minutes for the 1st 15 minutes and at every 30 minutes till it recedes to S2
Secondary Outcome Measures
NameTimeMethod
hemodynamic disturbance and complications.Timepoint: vital parameters will be monitored from 0 minute at 3 minute interval till 1st 15 minutes, at 10 minutes interval during the surgery and at 30 minutes interval till complete recovery. fall in MAP or SBP more than 30% or heart rate below 50/min requiring pharmacological treatment will be noted and patient followed up for 24 hours to note other complications such as nausea vomiting, rashes, urinary retention if any;onset and duration of motor blockTimepoint: motor block will be monitored from 0 minute at 30 seconds interval till grade 3 block according to modified Bromage scale is achieved and at 30 minutes interval till complete regression of motor block
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