Assessment of Blood Coagulation Disorders in Patients With Pulmonary Hypertension

Sponsor
National and Kapodistrian University of Athens (Other)
Overall Status
Unknown status
CT.gov ID
NCT03195543
Collaborator
(none)
60
1
68.7
0.9

Study Details

Study Description

Brief Summary

The objective of the present study is to assess blood coagulation disorders in patients with Pulmonary Arterial Hypertension and Chronic Thromboembolic Pulmonary Hypertension. The investigators aim to evaluate any possible coagulation abnormalities related to the patients' primary disease and any possible effects the pulmonary hypertension- specific therapy may have on hemostasis.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Platelet function analyzer-100
  • Diagnostic Test: Light transmission aggregometry
  • Diagnostic Test: Rotational thromboelastometry
  • Diagnostic Test: Endogenous thrombin potential

Detailed Description

Pulmonary hypertension (PH) is a chronic, progressive, pulmonary vascular disease with a multifactorial etiology and a not fully elucidated pathophysiological background. There is a complex and not adequately understood association between PH and the coagulation process.

The aim of the present study is to evaluate hemostasis in patients with PH classified as category 1 of the World Health Organization Pulmonary Hypertension Group (Pulmonary Arterial Hypertension, PAH) and 4 (Chronic Thromboembolic Pulmonary Hypertension, CTEPH). Patients with CTEPH are diagnosed as inoperable. The investigators perform diagnostic tests on blood samples collected directly from the pulmonary artery during the right heart catheterization performed as part of the patients' routine medical care for the diagnosis of the disease or for follow-up 6 months after the initiation of PH-specific treatment. All blood samples are processed by platelet function analyzer-100 (PFA-100), light transmission aggregometry (LTA), rotational thromboelastometry (ROTEM) and endogenous thrombin potential (ETP).The primary objective of the study is to assess platelet function, coagulation and anti-coagulation pathways and fibrinolysis in PAH and inoperable CTEPH patients and to investigate the possible effects of PH- specific therapy on hemostasis.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessment of Blood Coagulation Disorders in Patients With Pulmonary Arterial Hypertension and Chronic Thromboembolic Pulmonary Hypertension.
Actual Study Start Date :
Mar 12, 2015
Anticipated Primary Completion Date :
Dec 1, 2020
Anticipated Study Completion Date :
Dec 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Patients with PAH

Diagnostic tests will be performed on patients with Pulmonary Artery Hypertension in order to assess any blood coagulation disorders. Platelet function, coagulation and fibrinolysis will be evaluated by platelet function analyzer-100 (PFA-100), light transmission aggregometry, rotational thromboelastometry (ROTEM) and endogenous thrombin potential.

Diagnostic Test: Platelet function analyzer-100
The PFA-100 system evaluates primary hemostasis in whole blood samples.
Other Names:
  • PFA-100
  • Diagnostic Test: Light transmission aggregometry
    Light transmission aggregometry is the gold standard method for assessing platelet function.

    Diagnostic Test: Rotational thromboelastometry
    ROTEM is a viscoelastic method for hemostasis testing in whole blood.This assay investigates the interaction of blood cells, coagulation factors and their inhibitors during clotting and subsequent fibrinolysis.
    Other Names:
  • ROTEM
  • Diagnostic Test: Endogenous thrombin potential
    The endogenous thrombin potential assesses the amount of thrombin which can be generated after the in vitro activation of coagulation and represents the balance between pro- and anti-coagulant forces in plasma.
    Other Names:
  • ETP
  • Patients with CTEPH

    Diagnostic tests will be performed on patients with Chronic Thromboembolic Pulmonary Hypertension in order to assess any blood coagulation disorders. Platelet function, coagulation and fibrinolysis will be evaluated by platelet function analyzer-100 (PFA-100), light transmission aggregometry, rotational thromboelastometry (ROTEM) and endogenous thrombin potential.

    Diagnostic Test: Platelet function analyzer-100
    The PFA-100 system evaluates primary hemostasis in whole blood samples.
    Other Names:
  • PFA-100
  • Diagnostic Test: Light transmission aggregometry
    Light transmission aggregometry is the gold standard method for assessing platelet function.

    Diagnostic Test: Rotational thromboelastometry
    ROTEM is a viscoelastic method for hemostasis testing in whole blood.This assay investigates the interaction of blood cells, coagulation factors and their inhibitors during clotting and subsequent fibrinolysis.
    Other Names:
  • ROTEM
  • Diagnostic Test: Endogenous thrombin potential
    The endogenous thrombin potential assesses the amount of thrombin which can be generated after the in vitro activation of coagulation and represents the balance between pro- and anti-coagulant forces in plasma.
    Other Names:
  • ETP
  • Outcome Measures

    Primary Outcome Measures

    1. PFA-100 in detection of platelet abnormalities in PAH and CTEPH patients. [6 months]

      Change in the percentage of PAH and CTEPH patients who are detected with platelet abnormalities in PFA-100 testing from the date of the first right heart catheterization performed for the diagnosis of their disease (before treatment implementation) to the date of the second right heart catheterization performed for follow-up (after treatment implementation) at 6 months.

    2. Light transmission aggreggometry in detection of platelet abnormalities in PAH and CTEPH patients. [6 months]

      Change in the percentage of PAH and CTEPH patients who are detected with platelet abnormalities in LTA testing from the date of the first right heart catheterization performed for the diagnosis of their disease (before treatment implementation) to the date of the second right heart catheterization performed for follow-up (after treatment implementation) at 6 months.

    3. ROTEM in detection of coagulation abnormalities in PAH and CTEPH patients. [6 months]

      Change in the percentage of PAH and CTEPH patients who are detected with coagulation abnormalities in ROTEM testing from the date of the first right heart catheterization performed for the diagnosis of their disease (before treatment implementation) to the date of the second right heart catheterization performed for follow-up (after treatment implementation) at 6 months.

    4. Endogenous thrombin potential in detection of thrombin abnormalities in PAH and CTEPH patients. [6 months]

      Change in the percentage of PAH and CTEPH patients who are detected with thrombin deficits in endogenous thrombin potential testing from the date of the first right heart catheterization performed for the diagnosis of their disease (before treatment implementation) to the date of the second right heart catheterization performed for follow-up (after treatment implementation) at 6 months.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Pulmonary Arterial Hypertension,

    • Chronic Thromboembolic Pulmonary Hypertension.

    Exclusion Criteria:
    • renal insufficiency,

    • hepatic insufficiency,

    • thyroid dysfunction,

    • malignancy,

    • active infections,

    • receiving anticoagulant or antiplatelet therapy,

    • history of hemostatic disorders irrelevant to their primary disease,

    • abnormal red blood counts.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Attikon University Hospital Athens Greece 12462

    Sponsors and Collaborators

    • National and Kapodistrian University of Athens

    Investigators

    • Principal Investigator: Eleni Vrigkou, MD, MSc, National and Kapodistrian University of Athens
    • Study Director: Argyrios Tsantes, MD, PhD, National and Kapodistrian University of Athens
    • Study Chair: Iraklis Tsagkaris, MD, PhD, National and Kapodistrian University of Athens
    • Study Chair: Apostolos Armaganidis, MD, PhD, National and Kapodistrian University of Athens

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Eleni Vrigkou, PhD candidate, National and Kapodistrian University of Athens
    ClinicalTrials.gov Identifier:
    NCT03195543
    Other Study ID Numbers:
    • ΕΒΔ410/17-9-14
    First Posted:
    Jun 22, 2017
    Last Update Posted:
    Mar 25, 2019
    Last Verified:
    Mar 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Eleni Vrigkou, PhD candidate, National and Kapodistrian University of Athens
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 25, 2019