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A clinical study to compare success rate for block performed using ultrasound and x-ray after spine surgeries.

Not Applicable
Completed
Conditions
Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system
Registration Number
CTRI/2020/11/028839
Lead Sponsor
SRM Medical College Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
90
Inclusion Criteria

1. Patient undergoing lumbar spine surgery

2. ASA 1 and 2

Exclusion Criteria

1. Uncontrolled systemic illness, cardiac, renal and hepatic diseases

2. Patients not willing for the procedure

3. Patients allergic to Local Anaesthetic

4. Duration of surgery more than 3 hours

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the success rate between the two blocksTimepoint: The success rate will be assessed 30 minutes after extubation
Secondary Outcome Measures
NameTimeMethod
Duration of postoperative analgesiaTimepoint: The duration of postoperative analgesia is defined as the time taken <br/ ><br>from completion of block to the time when patient complaints of pain with VAS more than 3.;Total Morphine consumption in 24 hoursTimepoint: The total consumption of morphine in PCA pump for 24 hours will be noted
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