Comparison of pain relief of ultrasound guided cervical medial branch block

Comparison of pain relief of ultrasound guided cervical medial branch block using one level vs. two level injections

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009536

Enrollment

Registered

2024-06-14

Start date

2024-06-25

Completion date

Unknown

Last updated

2025-01-06

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

Conditions

None listed

Interventions

Procedure/Surgery : one level or two level medial branch block is performed at one group or another group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) 20-80 years (2) Cervical facet osteoarthritis (3) Cervical foraminal stenosis combining facet osteoarthritis

Exclusion criteria

Exclusion criteria: (1) patient who received cervical spinal surgery or trauma 1 year previoously (2) use of analgesics 24 hours before MBB (3) patient who is hard to fill in neck disability index (4) patient who has anatomical defect in the spot of procedure (5) patient who has bleeding tendency (6) pregnancy (7) patient who has an allergy to local anesthetics

Design outcomes

Primary

Measure	Time frame
numerical rating scale;neck disability index	—

Secondary

Measure	Time frame
procedure time ;procedure pain	—

Countries

Korea, Republic of

Contacts

Public ContactJiHee Hong

Keimyung University

swon13@daum.net+82-53-258-7767

Outcome results