Early Detection of Supraclavicular Brachial Plexus Block Failure Using Infrared Thermography and Perfusion Index

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorAssiut University

About this trial

Successful peripheral nerve blockade is fundamental to modern regional anesthesia, particularly for upper limb surgeries. Ensuring the efficacy of a nerve block early in the perioperative period is critical, as delayed recognition of block failure may lead to intraoperative pain, the need for additional sedation or general anesthesia, and overall poorer patient outcomes. Conventional methods for assessing block success, such as sensory testing with pinprick or cold stimuli and motor assessment using strength scales, require patient cooperation and often take 15-30 minutes to yield definitive results. These delays are especially limiting in fast-paced surgical environments or when early decisions regarding anesthesia management are necessary.

Emerging non-invasive monitoring technologies offer promising alternatives for the early, objective assessment of block efficacy. Infrared Thermography (IRT) measures skin surface temperature, which increases due to sympathetic nerve blockade-induced vasodilation.

Eligibility criteria

Qualifiers

Adults aged 18-70 years

ASA Physical Status I-III

Disqualifiers

General

Coagulopathy

Allergy to local anesthetics

Special

Trial design

Treatments tested in this trial

  • Ultrasound-Guided Supraclavicular Block
  • Bupivacaine Hydrochloride 0.5 % Injectable Solution
  • Ultrasound
  • Infrared Thermography Camera
  • Pulse Oximeter

Treatment groups

80 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators