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A randomised double blind trial to study the effectiveness and success rate of USG versus fluoroscopy(X-ray) guided caudal epidural steroid injections in adult patients with more than 3 months of radicular lower back pai

Phase 4
Conditions
Health Condition 1: M472- Other spondylosis with radiculopathy
Registration Number
CTRI/2024/06/069354
Lead Sponsor
il
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Adult patients 18 years of age  

2.Patients with chronic radicular lower back pain (not responding to conservative treatment like physical therapy, muscle relaxant drugs, or non-steroidal anti-inflammatory drugs for 6 weeks) 

3.Patients who are not candidates for surgical intervention.

Exclusion Criteria

Patients with

Local or systemic infection.

History of allergy to contrast.

Coagulopathy or anticoagulant therapy.

Progressive neurological deficit, motor weakness, sensory loss, cauda equina syndrome, bowel & bladder dysfunction.

Low back pain with traumatic aetiology, chronic nonradicular lower back pain.

Pregnant females.

Patients who refused to participate in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the pain relief at 1 month and procedure time with ultrasound versus fluoroscopy-guided caudal epidural steroid injections.Timepoint: 1 month
Secondary Outcome Measures
NameTimeMethod
The following outcome measures will be measured <br/ ><br>A)Pain relief in patients will be measured using NRS <br/ ><br>B)Improvement in disability index in patients will be measured using the ODI <br/ ><br>C) For measuring improvement in quality of life will be using the SF-12 score <br/ ><br>D)For measuring patient satisfaction will be using the Likert scale <br/ ><br>E) Adverse reactions if any e.g., facial flushing, infection etc. will be noted and reportedTimepoint: At 2 weeks, 1 month and 3 months
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