Comparison of terminal branch block and 3 nerve bundle block in ultrasound-guided axillary brachial plexus block for upper extremity surgery.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007460

Enrollment

Registered

2022-06-29

Start date

2022-04-25

Completion date

Unknown

Last updated

2022-09-20

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 : Anesthesia method for test group/control group: Experimental group uses the axillary artery peri-axillary injection method, and the control group uses the peri-neuronal injection m

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: # Selection criteria: 1) Patients receiving anesthesia by axillary brachial plexus block for surgery in the area below the elbow. 2) Adult male or female over the age of 19 3) The patient who signed the subject consent form.

Exclusion criteria

Exclusion criteria: # Exclusion criteria: 1) 80 years of age or older 2) Patients taking anticoagulants or prone to bleeding. 3) pregnant women 4) Patients whose consciousness is not clear or it is difficult to adequately answer the questionnaire 5) Patients taking pain medication for neuropathic pain and other diseases 6) If you have a history of allergy to local anesthetics 7) Infection at the site where anesthesia injection will be performed

Design outcomes

Primary

Measure	Time frame
anesthetic procedure time, sensory/motor nerve block time	—

Secondary

Measure	Time frame
complications caused by anesthetic procedure	—

Countries

Korea, Republic of

Contacts

Public ContactJaegyok Song

Dankook Univeristy Hospital

drjack@nate.com+82-41-550-6819

Outcome results