Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT06825819

Dysbiosis & Long COVID

Led by University of Chicago · Updated on 2026-03-02

400

Participants Needed

1

Research Sites

205 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The SARS-CoV-2 virus causes COVID-19, which ranges from mild initial symptoms to severe multi-organ dysfunction. While some patients recover to their baseline states, others develop a long COVID, or post-acute sequelae of SARS-CoV-2 (PASC) consisting of symptoms persisting \>2-6 months post-infection. PASC symptoms include post-exertional malaise, fatigue, and heart palpitations as well as incident GI disorders, cognitive dysfunction, and arthritis. Based on prevalence/incidence studies, it is estimated that more than 30 million people in the US have ever developed PASC with 10-11% of patients or 11 million people continuing to feel symptoms to the present day10. SARS-CoV-2 vaccines are only \~32% effective against infection at 4 months post-vaccination11, only 15% effective against the development of PASC12, and only 20% of American adults have received an updated booster as of December 202313. It is therefore imperative that the scientific community make progress in identifying underlying causes of PASC to develop effective treatments. This study will identify microbial metabolites associated with PASC-mediated gut dysbiosis and establish a tractable in vitro model to test T cell-gut epithelium dynamics to develop novel bio-therapeutics for multiple post-viral conditions. This case-control study will collect biospecimens (matched stool \& blood) samples from 400 people with and without long COVID (200 participants/group) to understand how COVID-induced dysbiosis impacts symptom severity, immune suppression, and gut barrier dysfunction both ex vivo and in vitro.

CONDITIONS

Official Title

Dysbiosis & Long COVID

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years
  • Any sex
  • Any race
  • Last COVID-19 infection confirmed by PCR or antigen test within the past 3 years, with symptoms (mild, moderate, or severe)
  • Any COVID vaccination status
  • Presence or absence of long COVID symptoms including gastrointestinal, cardiac, pulmonary, neurological, musculoskeletal, or psychological symptoms as defined by SBQ-LCTM
  • May or may not be undergoing routine endoscopy at UCM
Not Eligible

You will not qualify if you...

  • Age under 18 or over 80 years
  • Last confirmed COVID-19 infection occurred more than 3 years ago
  • Currently or within the past 3 months tested positive for COVID-19 by PCR or antigen test
  • Currently diagnosed with cancer
  • Currently pregnant (eligible only for survey, blood, and stool collection; colon biopsy not possible)
  • Currently taking biologic immunomodulatory medications
  • Official diagnosis of irritable bowel disease (IBD) or other chronic gastrointestinal disorder
  • Includes healthy adult volunteers, pregnant people, UCMC and UChicago employees, and staff/faculty as vulnerable or special populations

AI-Screening

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Trial Site Locations

Total: 1 location

1

The University of Chicago

Chicago, Illinois, United States, 60637

Actively Recruiting

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Research Team

L

Lavanya Visvabharathy, Ph.D

CONTACT

L

Leila Yazdanbakhsh, MSCI

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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