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Stellate Ganglion Blockade in COVID-19 Positive Patients

ARDS Clinical Trial

Official title:
Stellate Ganglion Blockade in COVID-19 Positive Patients

Clinical Trial Summary

This study will establish the safety and efficacy of using stellate ganglion blocks in patients with ARDS due to COVID-19 disease.

Clinical Trial Description

The attending proceduralist will perform the SGB in the ICU. Nurse will provide patient monitoring and assistance during the procedure. Standard monitors and ACLS resuscitative equipment will be immediately available. A norepinephrine solution will be at bedside to treat potential hypotension associated with SGB. The SGB perineural catheter will be placed using standard sterile technique. Initial perineural bolus injection - clonidine 100 mcg, Decadron PF 5mg, and 0.25% bupivacaine 5 ml is delivered. An OnQ perineural infusion 0.2% bupivacaine will be initiated at 2ml/hr for 5 days. Acute pain service will discontinue infusion and remove the catheter after 5 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04445337
Study type Interventional
Source University of Nebraska
Contact
Status Completed
Phase N/A
Start date November 15, 2020
Completion date November 1, 2021
View Details
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