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Comparison of Costoclavicular Brachial Plexus Block and Supraclavicular Brachial Plexus Block

Comparison of Costoclavicular Brachial Plexus Block and Supraclavicular Brachial Plexus Block

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03097159
Acronym
BPB
Enrollment
0
Registered
2017-03-31
Start date
2017-05-01
Completion date
2018-03-31
Last updated
2018-07-03

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

Conditions

Phrenic Nerve Paralysis

Keywords

costoclavicular block

Brief summary

The investigator will compare Costoclavicular approach of infraclavicular block and supraclavicular block. Especially, the incidence of phrenic nerve palsy and the quality of block.

Detailed description

Costoclavicular brachial plexus block is a recently developed approach of infraclavicular brachial plexus block. Using ultrasound, all of 3 cords are well visible in single plane. Compared to conventional infraclavicular block, it needs smaller amount of local anesthetics. Supraclavicular brachial plexus block is known as spinal anesthesia of upper extremities. It provides fast and good quality of anesthesia and analgesia. But some studies showed that there are over 50% of phrenic nerve palsy in supraclavicular block. In this study, the investigator will compare phrenic nerve palsy incidence and block quality between Costoclavicular block and supraclavicular block using ultrasound.

Interventions

Group C for costoclavicular block Group S for supraclavicular block

Sponsors

Ajou University School of Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* ASA I or II * Scheduled for surgery of hand or forearm

Exclusion criteria

* Patient refusal * Neuromuscular disease * Pregnancy * Previous history of surgery of periclavicular region * Nerve injury history * Bleeding tendency * Allergy to local anesthetics * Other contraindication of regional anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Diaphragm palsy30 minUsing M-mode of ultrasound, compare diaphragm movement pre-block and 30min after block Paralysis : reduced movement more than 75% or paradoxical movement on sniffing Paresis : 25\ 75% movement Normal : reduced less than 25%

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026