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An International Observational Study of Adults With Acute Infection

RecruitingObservational study

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age ≥18 years old
* Admitted to hospital (or in an emergency department with anticipated hospital admission) for the management of a suspected or confirmed acute infectious disease.
* Onset of symptoms of an infectious disease within the past 30 days.
* Informed consent for study participation by the participant or a surrogate decision maker if the participant lacks capacity for consent.

Exclusion Criteria:

* Current imprisonment (this does not include quarantine for an infectious disease).
* Patient undergoing comfort care measures only such that treatment focuses on end- of-life symptom management over prolongation of life.
* Expected inability or unwillingness to participate in study procedures.
* In the opinion of the investigator, participation in the study is not in the best interest of the patient.

About the study

Prospective, longitudinal studies of people with acute infections are essential to understand risk factors, clinical manifestations, pathobiology, and management strategies. Observational studies can provide data necessary to select interventions and strategies for testing in clinical trials and to develop key design features of trials. Observational studies can be particularly important for establishing an early knowledge base after emergence of a new pathogen, as illustrated by the recent emergence of influenza A (H1N1), SARS-CoV-2, and Mpox. This observational study protocol describes collection of data and biospecimens from sites across the world for characterizing acute infections in hospitalized patients. The protocol is designed to study respiratory infections, infections outside the respiratory tract, established infectious diseases, and emerging infectious diseases. Data generated in this study will be used to efficiently characterize acute infectious diseases and plan future clinical trials.

What is being tested

Sponsor: University of Minnesota · Participants: 1,500 · Started: Aug 25, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07069400

Locations in the U.S.

ArizonaBanner University Medical Center Tucson, Tucson
CaliforniaStanford University Hospital & Clinics (Site 203-003), Palo Alto
UCSF Medical Center (Site 203-001), San Francisco
FloridaOrlando VA Medical Center (074-032), Orlando
IllinoisUniversity of Illinois at Chicago (Site 008-012), Chicago
IndianaLutheran Medical Group, Fort Wayne
KansasUniversity of Kansas Medical Center (Site 080-044), Kansas City
MinnesotaUniversity of Minnesota, Minneapolis (Not yet recruiting)
Mayo Clinic (Site 054-001), Rochester
NebraskaUniversity of Nebraska Medical Center (Site 080-045), Omaha
New YorkMount Sinai Medical Center (Site 301-012), New York
New York University Langone Health (301-013), New York
North CarolinaDuke University (301-006), Durham
Wake Forest Baptist Health (210-001), Winston-Salem
OhioCleveland Clinic Foundation (Site 207-001), Cleveland
TennesseeVanderbilt University Medical Center (Site 212-001), Nashville
TexasUT Southwestern Medical Center (084-001), Dallas
MEDVAMC (Site 074-006), Houston
UtahIntermountain Medical Center (Site 211-001), Murray
West VirginiaWest Virginia University Medicine (301-023), Morgantown

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.