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A Randomized Comparison Between Conventional and Costoclavicular Ultrasound-Guided Infraclavicular Blocks

A Randomized Comparison Between Conventional and Costoclavicular Ultrasound-Guided Infraclavicular Blocks

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20160525001
Enrollment
90
Registered
2016-05-25
Start date
2016-09-08
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

Regional anesthesia Infraclavicular brachial plexus block Anesthesia Analgesia

Interventions

US probe will be appliedin the lateral infraclavicular fossa&#44
medial to the coracoid process&#44
to obtain a short&#45
axis view of the axillary artery. A 22&#45
gauge block needle will be advanced under direct US vision until the tip is located dorsal to the artery. ,US probe will be applied parallel to the lateral half of the clavicle&#44
gauge block needle will be advanced under direct US vision until the tip is positioned between the lateral&#44
medial and posterior cords.
Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery
Conventional group,Costoclavicular group

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: - Patients undergoing upper extremity surgery (elbow and below). - American Society of Anesthesiologists classification 1-3 - Body mass index between 18 and 30 kg/m2

Exclusion criteria

Exclusion criteria: - pre existing neuropathy or coagulopathy - renal failure or hepatic failure - allergy to local anesthetics - pregnancy - prior surgery in the area of the infraclavicular fossa - chronic pain syndromes requiring opioid intake at home

Design outcomes

Primary

MeasureTime frame
Onset time within 30 minutes after the end of the procedure Record the time from the end of local anesthetic drug injection to successful brachial plexus block

Secondary

MeasureTime frame
Performance time within 20 minutes after starting the procedure Record the time from applying ultrasound probe on skin to the end of local anesthetic drug injection,Total anesthesia-related time (sum of performance and onset times) within 30 minutes after the end of the procedure Record the time from applying ultrasound probe on skin until successful brachi plexus block achieved,Complications within 60 minutes after the end of the procedure Record incidences of intravascular injection, systemic toxic, pneumothorax, diaphragm paralysis.,Number of needle passes during the procedure Record number of needle passes used to reach the target,Procedural discomfort at the end of the procedure Use visual analog scale from 0 to 10

Countries

Thailand

Contacts

Public ContactPrangmalee Leurcharusmee

Chaing Mai University

prangmalee.l@cmu.ac.th6653935522

Outcome results

None listed

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