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NCT07012291 · ClinicalTrials.gov registry record

Clinical Performance Evaluation of Native Whole Blood Samples of Patients on DOACs With the Perosphere ClotChek™

A clinical trial of Coagulation, sponsored by Perosphere Technologies.

Recruiting
Registry status
150
Enrollment target
4
Study locations

NCT07012291: Recruiting study of Coagulation, sponsored by Perosphere Technologies.

NCT07012291 is a study of Coagulation that is actively recruiting participants, run by Perosphere Technologies. The registered enrollment target is 150 participants. The trial reports 4 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07012291, a study of Coagulation, is actively recruiting participants, sponsored by Perosphere Technologies.

RECRUITING
Registry status
150 participants
Enrollment target
4
Study locations

Study Summary

The Perosphere ClotChek™ system consists of a hand-held, battery-operated blood coagulation instrument and disposable test cuvettes for use at the point-of-care (POC). The instrument performs a whole blood clotting time (WBCT) test using freshly drawn, non-citrated whole blood. The purpose of the present study is to characterize the performance of the Perosphere ClotChek™ as a quantitative measurement of the WBCT in patients taking one of the following Direct Oral Anticoagulants (DOACs), rivaroxaban or apixaban.

Conditions Studied

Interventions

  • DEVICE Whole Blood Clotting Time

Study Locations (4)

Connecticut

  • Perosphere Technologies Inc - Danbury

Maryland

  • Perosphere Technologies Inc - Rockville

New Jersey

  • Eastern Vascular Associates - Denville

New York

  • Bassett Research Institute - Center for Clinical Research - Cooperstown

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2025-06-20
Est. Completion 2027-06-01
Perosphere Technologies

1 total trials

What NCT07012291 shows while recruiting

NCT07012291 is an observational study that tracks outcomes without assigning an intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap.

The record links to 1 condition, with Coagulation appearing as the primary indexed condition, and to 1 intervention - of which Whole Blood Clotting Time is the first listed.

NCT07012291 reports a single indexed study location in Connecticut, Maryland, New Jersey.

Frequently Asked Questions

What is clinical trial NCT07012291 about?

NCT07012291 is a clinical study titled "Clinical Performance Evaluation of Native Whole Blood Samples of Patients on DOACs With the Perosphere ClotChek™". The Perosphere ClotChek™ system consists of a hand-held, battery-operated blood coagulation instrument and disposable test cuvettes for use at the point-of-care (POC). The instrument performs a whole blood clotting time (WBCT) test using freshly drawn, non-citrated whole blood. The purpose of the pr...

What is the current status of trial NCT07012291?

This trial is currently recruiting. The enrollment target is 150 participants. The study started on 2025-06-20. Estimated completion is 2027-06-01.

What conditions does trial NCT07012291 study?

This clinical trial studies the following conditions: Coagulation.

What interventions are being tested in trial NCT07012291?

The interventions under investigation include: Whole Blood Clotting Time (DEVICE).

Who is sponsoring clinical trial NCT07012291?

This trial is sponsored by Perosphere Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07012291 being conducted?

This trial has 4 study locations across Connecticut, Maryland, New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07012291, the US trial registry maintained by the National Library of Medicine. NCT07012291 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.