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OpenTrials
Completed

NCT Number: NCT05812209

Stellate Ganglion Block to Treat Long COVID 19 Case Series

An assessment of the effectiveness of Stellate Ganglion Block in alleviating symptoms of Long COVID-19.

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Key information

About this study

We evaluated the treatment results of 41 patients (18 male and 23 female) aged between 18 and 89, who received Stellate Ganglion Block (SGB) with Ultrasound guidance for Long COVID-19 Syndrome. The patients were from the United States and received treatment at our Colorado clinics during the period of September to December 2022.Those who responded to our post-procedure follow-up calls were included in the study population.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

People who scheduled themselves for a SGB in our clinics in Colorado.

-

Exclusion criteria

Stellate Ganglion Block Contraindications

-

Treatment and study plan

Stellate ganglion block

Procedure

Ultrasound guided block of the Stellate Ganglion with local anesthetics.

Other names: SGB

Primary outcomes

  1. Symptom Response

    Time frame: 3 months

    Evaluation of the symptoms response to the Stellate Ganglion Block

Sponsors and collaborators

Lead sponsor

Metamorphosis LTD

Other

Registry information

Official study title

Stellate Ganglion Block to Treat Long COVID-19 Syndrome, A 41 Patient Retrospective Cohort Study

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Apr 13, 2023
Registry last updated
Apr 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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