Observational, Non-interventional Biomarker and Endotyping Study

Part of paid clinical trials in Urbana, Illinois.

Sponsor
Prenosis, Inc.
Study ID
NCT07675265
Status
Recruiting
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Conditions

  • ARDS (Acute Respiratory Distress Syndrome)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Study Details

The goal of this observational study is to establish a centralized ARDS biorepository of longitudinal biospecimens and harmonized clinical data, develop unsupervised, therapy-agnostic endotyping algorithms, and develop unsupervised, therapy-specific treatment-prediction algorithms over a 24 month period.

Key Dates

First listed
Jun 30, 2026
Start date
Sep 14, 2026
Status verified
Sep 2026
Primary completion
Dec 31, 2028
Completion
Mar 31, 2029

Study Design

Enrollment
1,200 participants (estimated)

Primary Outcome Measure

Number of Participants with an ARDS Diagnosis [ Time Frame: from enrollment to 28-day in-hospital mortality ]

Locations (1)

FacilityCityStateZIPSite coordinators
Carle Foundation HospitalUrbanaIllinois61801
Benjamin Davis, Associate Medical Director, MD
[email protected]
2173776109

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Carle Foundation Hospital· Urbana, IL

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