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A randomised controlled trial comparing cervical medial branch blocks by ultrasound-guided with combined bupivacaine and steroid versus bupivacaine alone for chronic cervical facet joint pai

Phase 3
Conditions
Chronic cervical facet joint pain patients
Cervical medial branch blocks
Chronic cervical facet joint pain
Ultrasond guidance
Registration Number
TCTR20210301008
Lead Sponsor
Mahidol University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
nknown
Sex
All
Target Recruitment
54
Inclusion Criteria

Patients who
1. 18 years of age
2. History of chronic, function-limiting neck pain of at least 3 months duration
3. Without radicular pain
4. Without a history of recent cervical surgical procedures within the last 3 months
5. Diagnosed chronic facet joint pain by cervical median branch block with 2% lidocaine and the pain intensity relief 50 % or more

Exclusion Criteria

Patients who
1. History of adverse reactions to local anesthetic or steroids
2. Uncontrolled major depression or psychiatric disorders
3. Acute or uncontrolled medical illness
4. Women who were pregnant or lactating
5. Heavy opioid usage defined as oral morphine equivalent more than 300 mg/day

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain at 1, 3 and 6 months after intervention Numberic rating scale
Secondary Outcome Measures
NameTimeMethod
eck disability index at 3 and 6 months after intervention Neck disability index
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