Stellate Ganglion Block to Treat Long COVID 19 Case Series

Sponsor
Metamorphosis LTD (Other)
Overall Status
Completed
CT.gov ID
NCT05812209
Collaborator
(none)
41
1
4
10.3

Study Details

Study Description

Brief Summary

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

Detailed Description

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.

Study Design

Study Type:
Observational
Actual Enrollment :
41 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Stellate Ganglion Block to Treat Long COVID-19 Syndrome, A 41 Patient Retrospective Cohort Study
Actual Study Start Date :
Sep 1, 2022
Actual Primary Completion Date :
Dec 31, 2022
Actual Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
SGB Patients for Long COVID 19

Patients who received ultrasound guided Stellate Ganglion block for symptoms of Long COVID in our Colorado clinics.

Procedure: Stellate Ganglion Block
Ultrasound guided block of the Stellate Ganglion with local anesthetics.
Other Names:
  • SGB
  • Outcome Measures

    Primary Outcome Measures

    1. Symptom Response [3 months]

      Evaluation of the symptoms response to the Stellate Ganglion Block

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

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

    -

    Exclusion Criteria:

    Stellate Ganglion Block Contraindications

    -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Metamorphosis LTD CaƱon City Colorado United States 81212

    Sponsors and Collaborators

    • Metamorphosis LTD

    Investigators

    • Principal Investigator: Lisa Pearson, DNAP, Metamorphosis LTD

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Lisa Pearson, Dr. Lisa Pearson, CRNA, NSPMc, Metamorphosis LTD
    ClinicalTrials.gov Identifier:
    NCT05812209
    Other Study ID Numbers:
    • SGBCOVID
    First Posted:
    Apr 13, 2023
    Last Update Posted:
    Apr 13, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 13, 2023