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NCT07382076: ACT

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

Active, enrolled Last updated 2 February 2026
What this trial tests

trial testing Blood draw in Activated Clotting Time in 500 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
15 December 2023
Primary endpoint
30 March 2026
30 March 2026

Quick facts

Lead sponsorAbbott Point of Care
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment500
Start date15 December 2023
Primary completion30 March 2026
Estimated completion30 March 2026
Sites11 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abbott Point of Care

Who can join

18 and older, any sex, with Activated Clotting Time. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Blood draw

Trials testing the same drug.

Other recruiting trials for Activated Clotting Time

Currently open trials in the same condition.

Other Abbott Point of Care trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07382076.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing