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sefulness of erector spinae blocks for spine surgeries

Not Applicable
Completed
Conditions
Health Condition 1: G968- Other specified disorders of central nervous system
Registration Number
CTRI/2021/11/038059
Lead Sponsor
Rajrajeshwari medical college and hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

ASA 1 patients

Exclusion Criteria

Coagulation disorders

BMI <18 or >30

Patient with surgical site infections

Patients with unstable spine integrity like fracture or scoliosis

Hypertensive, cardiac and diabetic patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study the efficacy of erector spinae block as an analgesia in lumbar decompression surgeriesTimepoint: To study the duration of action of erector spinae block as analgesia in lumbar decompression surgeries
Secondary Outcome Measures
NameTimeMethod
To study how much effectively erector spinae block reduces opiods, inhalation anesthetics and muscle requirements intraoperativelyTimepoint: 3 hrs
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