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Perfusion Index for Predicting Brachial Plexus Block Success Under General Anesthesia

Usefulness of Pulse Oximeter Perfusion Index for Predicting the Success of Interscalene Brachial Plexus Blockade Under General Anesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04925505
Enrollment
70
Registered
2021-06-14
Start date
2021-06-03
Completion date
2024-07-05
Last updated
2025-01-03

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

Conditions

Disorder of Shoulder

Brief summary

This study was designed to determine whether the success or failure of interscalene brachial plexus block under general anesthesia can be predicted using perfusion index (PI).

Detailed description

The success of peripheral nerve blocks is usually evaluated by assessment of sensory and motor function; however, this method cannot be applied in the patient who has uncheckable mental status, e.g. general anesthesia, or who is uncommunicable, e.g. different language user. The perfusion index (PI) is a numerical value for the ratio between pulsatile and non-pulsatile blood flow measured by a special pulse oximeter, and PI had been proved as a useful tool for evaluation of successful supraclavicular nerve block in awake patients as an objective method. With the use of ultrasound guidance in skilled hands, it is a reasonable option to perform neuraxial and peripheral regional blocks in sedated or anesthetized patients. However, there has been no evidence of applying PI for predicting the success of nerve block in general anesthetized patients.

Interventions

PROCEDUREInterscalene brachial plexus blocks with ultrasound guidance under general anesthesia

Ultrasound-guidance, interscalene brachial plexus blocks, in-plane technique, perineural injection, 0.5% ropivacaine 12.5ml and 0.2% lidocaine 12.5ml

Sponsors

Korea University Guro Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* 20-70 years old, * BMI 20-35 kg.m-2, * elective shoulder surgery, * ASA physical status I-III

Exclusion criteria

* refusal of the patient, * comorbid with serious vascular disease, * diabetes, * allergy to local anesthetics, * patients on regular opioids, * peripheral neuropathy.

Design outcomes

Primary

MeasureTime frameDescription
Perfusion Indexchange between before and 15 minutes after brachial plexus blockperfusion index measured applied to both blocked and non-blocked limbs using two separate oximeters

Secondary

MeasureTime frameDescription
Heart ratechange between before and 5 minutes after incision of surgical procedureheart rate in bpm during operation
Blood pressurechange between before and 5 minutes after incision of surgical procedureblood pressure in mmHg during operation
Pain score1 hour after surgeryNumeric rating scale for pain on a 0-10 scale where 0=no pain and 10=unbearable pain
Sensory function test on supraclavicular nerve and axillary nerve1 hour after surgery0-2 scale where 0=no block; 1=analgesia (patient can feel touch, not cold); 2=anesthesia (patient cannot feel touch)
Motor function test on supraclavicular nerve and axillary nerve and1 hour after surgery0-2 scale where 0 = no block; 1 = paresis; 2 = paralysis

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026