Long COVID Clinical Trial
— DSBLongCOVIDOfficial title:
Evaluating the Effectiveness of Dual Sympathetic Blocks for Patients Experiencing Sympathetically-Mediated Symptoms From Post-Acute Sequelae of SARS-CoV-2 (PASC)
Verified date | September 2023 |
Source | Hudson Medical |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this study is to gather data and assess changes in patient-reported outcomes with the stellate ganglion blocks as treatment for their sympathetically-mediated long COVID symptoms.
Status | Active, not recruiting |
Enrollment | 20 |
Est. completion date | December 30, 2023 |
Est. primary completion date | June 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: - Prior confirmed COVID-19 diagnosis by standard RT-PCR assay or equivalent testing - Persistent symptoms that continue four or more weeks after the start of a COVID-19 infection - Quantified autonomic symptoms from at least one domain as reported by the patient on the screener Composite Autonomic Symptom Score (COMPASS-31). The COMPASS-31 assesses 6 domains of autonomic symptoms: Orthostatic Intolerance, Vasomotor, Secretomotor, Gastrointestinal, Bladder, and Pupillomotor. - Quantified pain symptoms of pain interference or pain intensity as reported by the patient on the screener Patient-Reported Outcomes Measurement Information System (PROMIS-29) Exclusion Criteria: - Under age 18 - Prior SGB - Allergy to amide local anesthetics (e.g., ropivacaine, bupivacaine/Marcaine) - Pregnancy - Current anticoagulant use - History of a bleeding disorder - History of glaucoma - Infection or mass at injection site - For the consistency of this study, patients who deny all autonomic symptoms on the COMPASS-31 or pain symptoms on the PROMIS-29 will also be excluded |
Country | Name | City | State |
---|---|---|---|
United States | Hudson Medical | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Jonathann Kuo, MD |
United States,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient-Reported Outcomes: PROMIS-29 Score | The primary objective of the clinical effectiveness trial is to evaluate whether Dual Sympathetic Blocks performed at 0 and 1 weeks will improve patient-reported outcomes of depression, anxiety, physical function, pain interference, fatigue, sleep disturbance, and ability to participate in social roles and activities status. These domains are measured as reflected by Patient-Reported Outcomes Measurement Information System (PROMIS-29) total scores between baseline and 4 weeks | 1 month | |
Primary | Depression | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Anxiety | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Physical function | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Pain interference | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Fatigue | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Sleep disturbance | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Primary | Ability to participate in social roles and activities status | PROMIS-29 survey will measure changes in each domain scores between baseline and 4 weeks. | 1 month | |
Secondary | Autonomic Symptoms: COMPASS-31 Score | The secondary objective of the clinical effectiveness trial is to evaluate whether Dual Sympathetic Blocks performed at 0 and 1 weeks will improve Dysautonomia symptoms as reflected by corresponding Composite Autonomic Symptom Scale 31 (COMPASS-31) scores between baseline and 4 weeks | 1 month |
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