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Clinical Trials in Turkey / NCT07823738
Starting soon Not applicable

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

NCT07823738 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-10-15
Last updated
2026-09-21

Condition(s) studied

Nerve BlockRegional AnesthesiaUpper Extremity Surgery

Investigational drug(s) / intervention(s)

Classic Axillary BlockInterfascial Axillary Block

Classic Axillary Block: Classic (perivascular/perineural) axillary brachial plexus block

Interfascial Axillary Block: Interfascial (fascial-plane) axillary brachial plexus block.

Study 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).

Eligibility

Sex
ALL
Min age
18 Years
Max age
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bursa Yuksek Ihtisas Training and Research Hospital Bursa Turkey (Türkiye)

More Bursa Yuksek Ihtisas Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07823738 on ClinicalTrials.gov ↗ ← All trials in Turkey