Actively Recruiting

Age: 18Years +
All Genders
NCT06124612

An Investigator-initiated Linked Study to OCEANIC-AF

Led by East and North Hertfordshire NHS Trust · Updated on 2023-11-09

100

Participants Needed

2

Research Sites

149 weeks

Total Duration

On this page

Sponsors

E

East and North Hertfordshire NHS Trust

Lead Sponsor

L

Liverpool Heart and Chest Hospital NHS Foundation Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

Impaired endogenous fibrinolysis is a recently recognised risk factor for thrombotic events in patients with cardiovascular disease. Enhancing endogenous fibrinolysis in such individuals represents a way of reducing thrombosis risk. However, the optimal pharmacotherapy to enhance fibrinolysis is unclear. The aim of this study is to assess the effect of asundexian on endogenous fibrinolysis and compare this to apixaban. If asundexian can enhance endogenous fibrinolysis, this could be used as targeted treatment for patients who despite optimal antithrombotic therapy, demonstrate impaired endogenous fibrinolysis.

CONDITIONS

Official Title

An Investigator-initiated Linked Study to OCEANIC-AF

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or over
  • Patients enrolled in OCEANIC-AF study
  • Free from the exclusion criteria
  • Able and willing to understand the Patient Information Sheet and provide written informed consent
  • Agree to have blood samples drawn for assessments
Not Eligible

You will not qualify if you...

  • Unable to provide valid informed consent
  • Patients under 18 years of age
  • Significant neurological, hepatic, renal, endocrine, gastrointestinal, pulmonary, hemorrhagic, metabolic, or other diseases likely to affect the study
  • History or signs of substance abuse or active psychiatric disease
  • Alcohol consumption above 21 units per week
  • Any significant illness in the 4 weeks before screening
  • Major bleeding disorders or blood abnormalities as defined by specific blood test thresholds

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Liverpool Heart and Chest Hospital

Liverpool, United Kingdom

Not Yet Recruiting

2

East and North Herts NHS Trust

Stevenage, United Kingdom

Actively Recruiting

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Research Team

J

Joshua H Leader, MBCHB, BSc

CONTACT

D

Diana A Gorog, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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