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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 pain

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 pain

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210301008
Enrollment
54
Registered
2021-03-01
Start date
2021-03-15
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic cervical facet joint pain patients Cervical medial branch blocks Chronic cervical facet joint pain Ultrasond guidance

Interventions

0.5 % bupivacaine 4 ml plus normal saline 2 ml divided to 1 ml/injection site,0.5 % bupivacaine 4 ml plus dexamethasone 5 mg/ml 1 ml plus normal saline 1 ml divided to 1 ml/injection site
Active Comparator Drug,Active Comparator Drug
Bupivacaine,Bupivaciane and dexamethasone

Sponsors

Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Pain at 1, 3 and 6 months after intervention Numberic rating scale

Secondary

MeasureTime frame
Neck disability index at 3 and 6 months after intervention Neck disability index

Countries

Thailand

Contacts

Public ContactNiruji Saengsomsuan

Faculty of Medicine Siriraj Hospital, Mahidol University

jns_owen@hotmail.com024197842

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026