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A clinical study to know the effect of injection of normal saline through epidural catheter on the level of spinal anaesthesia in patients undergoing lower limb surgeries.

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/09/057943
Lead Sponsor
M S Rmaiah medical college
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

all patients undergoing elective lower limb surgeries under combined spinal epidural anaesthesia who fit into american society of anaesthesiologists (ASA) physical status I and II

Exclusion Criteria

american society of anaesthesiologist (ASA) physical status III and above

patient refusal

patients in whom CSEA is contraindicated

patients having allergy to drugs used in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
onset & duration of sensory blockade <br/ ><br>maximum level of sensory blockade achieved <br/ ><br>onset and duration of motor blockadeTimepoint: levels will be tested every minute until highest level is achieved & every 10 mins there after until 2 segment regression is achieved
Secondary Outcome Measures
NameTimeMethod
hypotension <br/ ><br>bradycardia <br/ ><br>side effects like nausea , vomiting , shiveringTimepoint: the hemodynamic parameters will be checked every 2mins interval for 1st 10mins, followed by ever 5mins for next 20 mins & every 10mins till the end of surgery
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