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Completed No phase listed Observational

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

ClinicalTrials.gov ID: NCT07382076

Public ClinicalTrials.gov record NCT07382076. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 2:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT07382076
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Abbott Point of Care
Industry
Enrollment
500 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 18, 2023 (Actual)
Primary completion
Feb 19, 2026 (Actual)
Completion
Feb 19, 2026 (Actual)
Last update posted
Oct 28, 2026

2023 – 2026

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Dignity Health Chandler Regional Medical Center Chandler Arizona 85224 —
University of California at San Francisco San Francisco California 94132 —
George Washington University Washington D.C. District of Columbia 20052 —
Kentucky Clinical Trials Laboratory Louisville Kentucky 40202 —
University of Maryland Baltimore Maryland 21201 —
Minneapolis Heart Institute Minneapolis Minnesota 55407 —
Washington University St Louis Missouri 63110 —
Icahn School of Medicine at Mount Sinai New York New York 10029 —
Penn State University Hershey Medical Center Hershey Pennsylvania 17033 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
Eastside Research Associates - Redmond Redmond Washington 98052 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07382076, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 28, 2026 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07382076 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →