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Looking for blood and tissue markers of Long COVID in adults

Studies samples from people with Long COVID and people recovered from COVID-19.

Plain-language title generated from the registry record
Registry title: Validation of Biomarkers for Long COVID in the LIINC Viral Immunopathogenesis and Persistence Repeat Donor Cohort (VIPER)

Key facts

Where
San Francisco, United StatesSee the site

Where in United States

  • Zuckerberg San Francisco General HospitalSan Francisco, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of California, San Francisco
Trial code
NCT07770022
Record updated
18 August 2026
Original description
The purpose of this study is to better understand the biological changes associated with Long COVID and to identify laboratory tests (biomarkers) that may help diagnose the condition and measure how it changes over time. Researchers will enroll people with Long COVID as well as people who have fully recovered after COVID-19 infection.Read full original descriptionShow less

Validation of Biomarkers for Long COVID in the LIINC Viral Immunopathogenesis and Persistence Repeat Donor Cohort (VIPER)

The purpose of this study is to better understand the biological changes associated with Long COVID and to identify laboratory tests (biomarkers) that may help diagnose the condition and measure how it changes over time. Researchers will enroll people with Long COVID as well as people who have fully recovered after COVID-19 infection.

Participants will provide health information and biological samples, such as blood, saliva, stool, and, for some participants, tissue biopsies. These samples will be used to study the biological processes involved in Long COVID and to support the development of new diagnostic tests that may improve future research, clinical trials, and patient care.

Inclusion: Willing and able to provide written informed consent, and; Age >/= 18 years, and; Either:; History of a SARS-CoV-2 infection resulting in Long COVID symptoms, confirmed by the investigator, or; Exposure to SARS-CoV-2 without establishment of Long COVID; Enrolled or willing to enroll and complete at least 1 visit in the UCSF Long-term Impact of Infection with Novel Coronavirus (LIINC); Enrolled or willing to be referred for a gut biopsy procedure under related IRB-approved protocols.

Exclusion: Serious medical or psychiatric illness that, in the opinion of the site investigator, would interfere with the ability to adhere to study requirements or to give informed consent; Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data; Self-reported or documented chronic anemia with hemoglobin < 9 g/dL. Anemia during a preceding acute illness will not be exclusionary.

ClinicalTrials.gov NCT07770022