About this trial
Hand, wrist, and forearm surgeries are commonly performed procedures with significant postoperative pain potential. Regional anesthesia of the brachial plexus via the axillary approach is one of the gold-standard techniques for distal upper-limb surgery. In the conventional (classic) axillary block, the median, ulnar, and radial nerves within the axillary sheath are individually targeted under ultrasound guidance; however, anatomical septations around the axillary artery may prevent homogeneous spread of local anesthetic, leading to a patchy block and reduced intraoperative success.
The interfascial axillary block is a modified approach in which local anesthetic is deposited into the fascial planes between the axillary muscles rather than directly into the nerve sheath, aiming for passive diffusion, homogeneous spread, and fewer needle manipulations. This prospective, randomized, single-center study compares the classic axillary block with the interfascial axillary block in patients undergoing hand, wrist, and forearm surgery, primarily in terms of surgical anesthesia adequacy (block success).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18-90 years
American society of anesthesiologists physical status I-II-III
Scheduled for elective hand, wrist, or forearm surgery
Written informed consent obtained
Disqualifiers
History of local anesthetic allergy
Coagulation disorder
BMI > 40 kg/m²
Infection at the block site
Trial design
Parallel
Treatments tested in this trial
Classic Axillary Block
Procedure/SurgeryClassic (perivascular/perineural) axillary brachial plexus block
Interfascial Axillary Block
Procedure/SurgeryInterfascial (fascial-plane) axillary brachial plexus block.
Treatment groups
Trial outcomes
Primary outcomes
Surgical anesthesia adequacy (block success)
Complete sensory and motor blockade of the surgical field, allowing the operation to be completed without additional local infiltration or conversion to general anesthesia
Secondary outcomes
Block application time
time from needle insertion to withdrawal.
Sensory block onset time
Pin-Prick test in the median, ulnar, radial, and musculocutaneous dermatomes (0: normal, 1: blunt, 2: no sensation).
Motor block onset time
Intraoperative additional analgesic/sedation consumption
Sponsors and contacts
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