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The Primary objective of this study is to determine, using unblinded samples, if it is possible to develop an algorithm for the classification of specific blood RNA from patients with long COVID together and separately from the apparent health normal controls and other medical conditions that share the signs and symptoms of long COVID.
Participants will be screened and provide two blood samples28 (+/- 2) days apart. Based on the participants survey results they will be placed into one of fourteen groups that reflect the type of Long COVID the patient is experiencing. Samples will be shipped to the sponsor who will develop an AI process to validate the type of Long COVID and assess its severity. The long term goal is to develop a reliable test to identify the presence of Long COVID and its severity.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of Iowa
Iowa City, Iowa, United States
The MaxWell Clinic
Brentwood, Tennessee, United States
The MaxWell Clinic
Brentwood, Tennessee, United States
Start Date
March 15, 2024
Primary Completion Date
March 15, 2026
Completion Date
March 15, 2026
Last Updated
October 18, 2024
224
ESTIMATED participants
RNA Biomarker Blood Test
DIAGNOSTIC_TEST
Lead Sponsor
MaxWell Clinic, PLC
NCT06721949
NCT06631287
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06086366