Skip to content

Comparative outcome of lidocaine and bupivacaine for cervical medial branch block in chronic cervical facet arthropathy: a randomized prospective study

compare outcome of lidocaine and bupivacaine for cervical medial branch block in chronic cervical facet arthropathy: a randomized prospective study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210404001
Enrollment
62
Registered
2021-04-04
Start date
2021-03-09
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 neck pain from fecet joint cervical medial branch block, cervical facet arthropathy, neck pain, lidocaine, bupivacaine

Interventions

2% lidocaine will be use in cervical medial branch block 0.5 ml per level of cervical spine (maximum 5 ml) using 25G needle under ultrasound guided.,0.5% bupivacaine will be use in cervical medial br
Active Comparator Drug,Active Comparator Drug
lidocaine,bupivacaine

Sponsors

Faculty of Medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. patient with non-specific neck pain without radicular pain for more than 3 months 2. patient with non-specific neck pain without radicular pain for more than 3 months who are not improve after receiving medical treatment. (not improve define as numeric rating scale more than 4 or pain disturb function in daily life) 3. MRI finding dose not find surgical condition 4. positive result from diagnostic block

Exclusion criteria

Exclusion criteria: 1. negative result from diagnostic block 2. allergic to lidocaine or bupivacaine 3. have local infection at the area proceeding the procedure 4. coagulopathy 5. chronic neck pain from malignancy 6. unstable and severe underlying disease

Design outcomes

Primary

MeasureTime frame
duration of 50 percent pain relief every week until 50 percent pain relief week (interview)

Secondary

MeasureTime frame
duration of 75 percent pain relief every week until 75 percent pain relief week (interview),number of patient with 50% pain relief at recovery room 30 minutes after procedure interview,number of patient with 50% pain relief at 2 weeks 2 weeks after procedure interview,number of patient with 50% pain relief at 1 month 1 month after procedure interview,number of patient with 50% pain relief at 3 months 3 months after procedure interview,number of patient with 75% pain relief at recovery room 30 minutes after procedure interview,number of patient with 75% pain relief at 2 weeks 2 weeks after procedure interview,number of patient with 75% pain relief at 1 month 1 month after procedure interview,number of patient with 75% pain relief at 3 months 3 months after procedure interview,neck disability index at 2 week 2 weeks after procedure neck disability index questionnaire,neck disability index at 1 month 1 month after procedure neck disability index questionnaire,neck disability index at 3 months 3 months after procedure neck disability index questionnaire

Countries

Thailand

Contacts

Public ContactPorntipa Pasuhirunnikorn

Faculty of Medicine, Chulalongkorn University

porntipa.pasu@gmail.com022564000

Outcome results

None listed

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