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NCT03207451 · ClinicalTrials.gov registry record · Phase 4

Vorapaxar on Thrombin Generation and Coagulability

A Phase 4 study, sponsored by Inova Health Care Services.

Completed
Registry status
Phase 4
Development phase
81
Enrollment target

NCT03207451: Completed Phase 4 study, sponsored by Inova Health Care Services.

NCT03207451 is a Phase 4 study that has completed, run by Inova Health Care Services. The registered enrollment target is 81 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03207451, a Phase 4 study, has completed, sponsored by Inova Health Care Services.

COMPLETED
Registry status
Phase 4
Development phase
81 participants
Enrollment target

Study Summary

This investigation will be conducted in patients 18-75 years of age with multiple coronary artery disease risk factors (antiplatelet naïve patients) and patients with prior MI or PVD on antiplatelet therapy. Pharmacodynamics will be assessed at multiple time points to assess onset-, maintenance-, and offset-effect of vorapaxar on thrombin generation, platelet reactivity, and plasma/platelet endothelial and inflammatory biomarkers. Safety assessment will be assessed throughout the study.

Primary Outcome

15 μmol/L SFLLRN (PAR-1 activating peptide) induced maximum platelet aggregation at 30 days after treatment with Vorapaxar

Interventions

  • DRUG Vorapaxar
  • DRUG Vorapaxar and Aspirin
  • DRUG Vorapaxar and Clopidogrel
  • DRUG Vorapaxar, Aspirin, and Clopidogrel

Trial Details

FieldValue
Enrollment Target 81 participants
Start Date 2016-01-01
Est. Completion 2018-08-01
Phase Phase 4
Inova Health Care Services

75 total trials

What the finished NCT03207451 record still lists

NCT03207451 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 81 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 4 interventions - of which Vorapaxar is the first listed.

NCT03207451 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03207451 about?

NCT03207451 is a clinical study titled "Vorapaxar on Thrombin Generation and Coagulability". This investigation will be conducted in patients 18-75 years of age with multiple coronary artery disease risk factors (antiplatelet naïve patients) and patients with prior MI or PVD on antiplatelet therapy. Pharmacodynamics will be assessed at multiple time points to assess onset-, maintenance-, an...

What is the current status of trial NCT03207451?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 81 participants. The study started on 2016-01-01. Estimated completion is 2018-08-01.

What interventions are being tested in trial NCT03207451?

The interventions under investigation include: Vorapaxar (DRUG), Vorapaxar and Aspirin (DRUG), Vorapaxar and Clopidogrel (DRUG), Vorapaxar, Aspirin, and Clopidogrel (DRUG).

Who is sponsoring clinical trial NCT03207451?

This trial is sponsored by Inova Health Care Services, which has 75 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03207451's enrollment target sits among peer trials

81 940th of 2000 higher than 1,055 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03207451, the US trial registry maintained by the National Library of Medicine. NCT03207451 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.