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Comparison of Costoclavicular block with Supraclavicular and Axillary block for Upper Limb Surgery: A Randomized Trial

Efficacy of surgical analgesia of Costoclavicular block in comparison to Supraclavicular and Axillary blockade, guided by ultrasonography, for procedures distal to the elbow: A randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9wzwv5
Enrollment
Unknown
Registered
2019-10-21
Start date
2019-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Multiple injuries of forearm

Interventions

54 participants with indication for surgery on the upper limb distal to the elbow will be selected and randomized by draw in two groups. Comparison group: 27 patients who will be submitted to costocla

Sponsors

Hospital das Clínicas da Universidade Federal de Uberlândia
Lead Sponsor
Hospital das Clínicas da Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Participants undergoing elective and urgent elbow, forearm, wrist and hand surgeries; both genres; aged 18 to 70 years; ASA I to III classification; BMI between 18 and 30

Exclusion criteria

Exclusion criteria: participant's refusal; classification of physical status ASA greater than III; inability to consent; coagulopathy; sepsis; pregnancy; neuromuscular disease; allergy to local anesthetics; neuropathy or previous deficit of musculocutaneous / radial / ulnar / median; previous surgery in the infraclavicular fossa; infection at the needle insertion site

Design outcomes

Primary

MeasureTime frame
We will evaluate the time for complete sensorimotor block by the costoclavicular brachial plexus block technique, comparing it with the control group with the axillary supraclavicular brachial plexus block technique, performing thermal sensory tests on radial nerve dermatomes, median, ulnar and musculocutaneous, at intervals of 5 minutes until the complete loss of thermal sensitivity of each dermatome;It will be evaluated the time to perform the blockade, the number of times it was necessary to reposition the needle to perform the procedure.

Secondary

MeasureTime frame
We will assess the adverse events associated with the techniques.;After 30 minutes of blockade, immobility, tactile and painful sensitivity related to each nerve will be evaluated. Immobility will be tested as follows: thumb abduction (n. Radial), elbow flexion (n. Musculocutaneous), thumb adduction (n. Ulnar) and thumb opposition (n. Median). Tactile sensitivity will be evaluated using the Semmes-Weinstein 300g monofilament and painful sensitivity through the Buck needle in each dermatome of the evaluated nerves

Countries

Brazil

Contacts

Public ContactRoberto Ruzi

Hospital das Clínicas da Universidade Federal de Uberlândia

anestesia@robertoruzi.com.br+55-034-32330531

Outcome results

None listed

Source: REBEC (via WHO ICTRP)