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NCT06006884Recruiting

A Study of Post COVID-19 Mechanisms for Chronic Lung Sequelae

Uncover Mechanisms Underlying the Development of Chronic Lung Sequelae Post COVID-19

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

The purpose of this study is to understand why some people experience long term effects, such as shortness of breath and fatigue, after a severe COVID-19 infection

Status (registry)
Recruiting
Study type
Observational
Enrollment
67 (estimated)
First submitted
22 Aug 2023
Start date
10 Jan 2024
Primary completion date
Aug 2027
Lead sponsor
Mayo Clinic
NCT number
NCT06006884

What you commit to

  • Study type: Observational
  • Planned participants: 67
  • From 10 Jan 2024 to the primary completion date, Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Immunocompromised host status due to ongoing therapy with methotrexate, CellCept, azathioprine, rituximab, cyclophosphamide or other biologic agents;

Other illness

  • Inability to provide informed consent, evidence of pre-existing interstitial lung disease or chronic lung disease;
  • History of chemotherapy or radiation therapy in the last two years; and pregnancy.

Other

  • Active cigarette smoking, vaping or other inhalation use.
  • \> 20 pack year smoking history.

Who the study is looking for

  • For the Sequelae Group
  • Age ≥18 years at screening, PCR confirmed COVID19 illness (+PCR defines day 0 of illness), hospitalization for COVID-19, absence of pre-existing history of interstitial lung disease, or significant other lung disease.
  • Severity of illness will be categorized as moderate disease (supplemental oxygen need 1-8L at any time during hospitalization), severe disease (need for high flow oxygen delivery ≥8L at any time during hospitalization) and critical illness (need for ICU admission or mechanical ventilation).
    • Control Recovery Group
  • Age ≥18 years at screening
  • PCR confirmed COVID-19 cases who had nonsymptomatic or mild acute infection that do not require hospitalization 7,48,49
  • Absence of pre-existing history of interstitial lung disease, or significant other lung disease, absence of any ongoing respiratory and systemic symptoms.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic Minnesota
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.