Skip to content

Classic Versus Interfascial Axillary Block in Hand, Wrist, and Forearm Surgery

Comparison of Axillary Block and Interfascial Axillary Block in Terms of Block Success and Intraoperative Clinical Efficacy in Hand, Wrist, and Forearm Surgery: A Prospective Randomized Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07823738
Enrollment
110
Registered
2026-09-16
Start date
2026-10-15
Completion date
2027-09-30
Last updated
2026-09-16

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

Conditions

Nerve Block, Regional Anesthesia, Upper Extremity Surgery

Keywords

axillary block, interfascial block, regional anesthesia

Brief summary

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).

Detailed description

This is a prospective, randomized, single-center clinical trial conducted in a Department of Anesthesiology and Reanimation. Randomization is performed using the sealed-envelope method. A total of 110 patients (55 per group) aged 18-90 years, American society of anesthesiologists physical status I-III, scheduled for elective hand, wrist, or forearm surgery under ultrasound-guided regional anesthesia will be enrolled. Group 1 (Classic Axillary Block) receives an ultrasound-guided block targeting the median, ulnar, and radial nerves perineurally/perivascularly within the axillary sheath. Group 2 (Interfascial Axillary Block) receives an ultrasound-guided injection of local anesthetic into the potential fascial planes between the axillary muscles, relying on passive diffusion. The primary outcome is surgical anesthesia adequacy (block success). Secondary outcomes include block application time, sensory and motor block onset, rates of additional local infiltration and conversion to general anesthesia, intraoperative additional analgesic/sedation requirements, hemodynamic parameters, patient and surgeon satisfaction, and complications.

Interventions

PROCEDUREClassic Axillary Block

Classic (perivascular/perineural) axillary brachial plexus block

PROCEDUREInterfascial Axillary Block

Interfascial (fascial-plane) axillary brachial plexus block.

Sponsors

Bursa Yuksek Ihtisas Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* 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

Exclusion criteria

* History of local anesthetic allergy * Coagulation disorder * BMI \> 40 kg/m² * Infection at the block site * Chronic pain syndrome * Pregnancy * Inability to communicate * Need for emergency surgery

Design outcomes

Primary

MeasureTime frameDescription
Surgical anesthesia adequacy (block success)30 minutes after blockComplete sensory and motor blockade of the surgical field, allowing the operation to be completed without additional local infiltration or conversion to general anesthesia

Secondary

MeasureTime frameDescription
Block application timeintraoperativetime from needle insertion to withdrawal.
Sensory block onset time5., 10., 15., 30. minutesPin-Prick test in the median, ulnar, radial, and musculocutaneous dermatomes (0: normal, 1: blunt, 2: no sensation).
Motor block onset time5., 10., 15., 30. minutes
Intraoperative additional analgesic/sedation consumptionintraoperative
Patient and surgeon satisfactionend of surgery4-point Likert scale (1: very poor, 4: very good)

Countries

Turkey (Türkiye)

Contacts

CONTACTKorgün Ökmen, PhD.
korgunokmen@gmail.com05057081021

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026