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ACTIVE NOT RECRUITING
NCT07382076

Clinical Evaluation of the i-STAT ACTpro Cartridge in an Adult Population

Sponsor: Abbott Point of Care

View on ClinicalTrials.gov

Summary

Measuring Activated Clotting Time (ACT) using the i-STAT ACTpro cartridge on the i-STAT 1 analyzer compared to a comparator device.

Official title: Clinical Evaluation of the i-STAT ACTpro Cartridge Using Venous and Arterial Whole Blood Specimens on the i-STAT 1 Analyzer in an Adult Population

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

500

Start Date

2023-12-15

Completion Date

2026-03-30

Last Updated

2026-02-02

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Blood draw

A total volume of no more than 5mL of blood will be prospectively collected from subjects.

Locations (11)

Dignity Health Chandler Regional Medical Center

Chandler, Arizona, United States

University of California at San Francisco

San Francisco, California, United States

George Washington University

Washington D.C., District of Columbia, United States

Kentucky Clinical Trials Laboratory

Louisville, Kentucky, United States

University of Maryland

Baltimore, Maryland, United States

Minneapolis Heart Institute

Minneapolis, Minnesota, United States

Washington University

St Louis, Missouri, United States

Icahn School of Medicine at Mount Sinai

New York, New York, United States

Penn State University Hershey Medical Center

Hershey, Pennsylvania, United States

Thomas Jefferson University

Philadelphia, Pennsylvania, United States

Eastside Research Associates - Redmond

Redmond, Washington, United States