Stellate Ganglion Block (SGB) for COVID-19 Acute Respiratory Distress Syndrome (ARDS)
NCT ID: NCT04402840
Last Updated: 2025-04-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
5 participants
INTERVENTIONAL
2020-04-24
2020-12-31
Brief Summary
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Detailed Description
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• To determine safety of stellate ganglion block (SGB) in ARDS
Secondary Aim:
* To determine efficacy of SGB in slowing the progression of ARDS
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Stellate Ganglion Block (SGB)
Clinical Stellate ganglion block
Stellate Ganglion Block
The procedure will be done at the bedside in the ICU without interfering with ongoing treatment.
Interventions
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Stellate Ganglion Block
The procedure will be done at the bedside in the ICU without interfering with ongoing treatment.
Eligibility Criteria
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Inclusion Criteria
* Subjects with PCR documented diagnosis of COVID-19 ARDS requiring critical care and transfer to intensive care unit
* Bilateral opacities consistent with pulmonary edema must be present and may be detected on CT or chest radiograph
Exclusion Criteria
* Hemodynamic Instability
* Subject on Extracorporeal membrane oxygenation (ECMO)
* Anatomical inability to do a stellate block
18 Years
80 Years
ALL
No
Sponsors
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West Virginia University
OTHER
Responsible Party
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Ali Rezai
Director
Principal Investigators
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Ali R Rezai, MD
Role: PRINCIPAL_INVESTIGATOR
West Virginia University
Locations
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West Virginia University Rockefeller Neuroscience Institute
Morgantown, West Virginia, United States
Countries
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Other Identifiers
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2004963113
Identifier Type: -
Identifier Source: org_study_id
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