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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ACTIVE_NOT_RECRUITING
200 participants
OBSERVATIONAL
2021-03-01
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Longhauler's Syndrome Cohort
Subject's with longhaulers
No interventions assigned to this group
Control Cohort
Control cohort will not have had a known case of COVID-19 or Longhauler's syndrome
No interventions assigned to this group
COVID Control Cohort
Subjects who have had COVID-19 but no known Longhauler's syndrome
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* At least 18 years old.
* Ability of subject or LAR to read and speak the English language.
* Positive PCR or antibody test within 12 months of initial study visit.
* Patient of the Long-Hauler Syndrome clinic and differential diagnosis of Long-Hauler Syndrome.
* Ability to give informed consent
* At least 18 years old
* Ability of subject to read and speak the English language
* Ability to give informed consent.
* At least 18 years old.
* Ability of subject to read and speak the English language.
* Known case of COVID-19.
Exclusion Criteria
* Pregnant females.
* Incarcerated individuals.
* Inability to cooperate or any medical condition that, in the opinion of the investigator, interferes with the evaluation of the study objectives or increases the subject's risk by participating in the study.
Control Cohort -
* Known case of COVID-19.
* Any potential participant who refuses medical record review.
* Pregnant females.
* Incarcerated individuals.
* Inability to cooperate or any medical condition that interferes with the evaluation of the study objectives or increases the subject's risk by participating in the study.
COVID-19 Control Cohort
* Known Longhauler's syndrome/Post-COVID
* Any potential participant who refuses medical record review.
* Pregnant females.
* Incarcerated individuals.
* Inability to cooperate or any medical condition that interferes with the evaluation of the study objectives or increases the subject's risk by participating in the study.
18 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Ryan T. Hurt, M.D., Ph.D.
Principal Investigator
Principal Investigators
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Ryan T. Hurt, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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20-011877
Identifier Type: -
Identifier Source: org_study_id
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