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Assessment of Blood Coagulation Disorders in Patients With Pulmonary Hypertension

Assessment of Blood Coagulation Disorders in Patients With Pulmonary Arterial Hypertension and Chronic Thromboembolic Pulmonary Hypertension.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03195543
Enrollment
60
Registered
2017-06-22
Start date
2015-03-12
Completion date
2020-12-31
Last updated
2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Thromboembolic Pulmonary Hypertension, Pulmonary Artery Hypertension

Keywords

Blood coagulation disorders, Platelets, Thrombin, Treatment

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.

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.

Interventions

DIAGNOSTIC_TESTPlatelet function analyzer-100

The PFA-100 system evaluates primary hemostasis in whole blood samples.

DIAGNOSTIC_TESTLight transmission aggregometry

Light transmission aggregometry is the gold standard method for assessing platelet function.

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.

DIAGNOSTIC_TESTEndogenous 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.

Sponsors

National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
PFA-100 in detection of platelet abnormalities in PAH and CTEPH patients.6 monthsChange 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.
Light transmission aggreggometry in detection of platelet abnormalities in PAH and CTEPH patients.6 monthsChange 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.
ROTEM in detection of coagulation abnormalities in PAH and CTEPH patients.6 monthsChange 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.
Endogenous thrombin potential in detection of thrombin abnormalities in PAH and CTEPH patients.6 monthsChange 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.

Countries

Greece

Contacts

Primary ContactEleni Vrigkou, MD, MSc
elenivrigkou@gmail.com00302105832179
Backup ContactArgyrios Tsantes, MD, PhD
atsantes@med.uoa.gr00302105830000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026