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Hemodynamic Changes in Connective Tissue Disease

Hemodynamic Changes in Connective Tissue Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01468792
Enrollment
85
Registered
2011-11-09
Start date
2011-09-30
Completion date
2014-02-28
Last updated
2014-02-19

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

Conditions

Systemic Sclerosis

Keywords

systemic sclerosis, pulmonary arterial hypertension

Brief summary

The study serves the identification of early forms of pulmonary arterial hypertension (PAH) in connective tissue disease and the hemodynamic follow-up of the investigated patients. The basic hypothesis is that PAH may start with a remodeling of small pulmonary arteries, which leads to a stiffening of the vessels, indicated by the inability to vasodilatation and thus a disproportional increase in pulmonary pressure during exercise. Recent studies have shown that a proportion of such patients may develop manifest PAH within a few years. The early identification of these patients and the understanding of the natural course of the disease may improve prognosis. The aim of the present study is to investigate hemodynamic and clinical changes in patients with connective tissue disease in a time interval of 3-5 years with a focus on the development of pulmonary hypertension.

Interventions

None listed

Sponsors

Medical University of Graz
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Informed consent * Patients with systemic sclerosis, mixed connective tissue disease, (systemic lupus erythematodes) SLE or overlap syndrome * Existing exercise Doppler echocardiography or/and right heart catheterization 3-5 years before inclusion

Exclusion criteria

* \- Severe lung or bronchial disease (FEV1 \<60%) * Systolic LV dysfunction (LVEF \<50%) or diastolic dysfunction \> grade I * Valvular defect \> grade I (except for tricuspid- or pulmonary insufficiency) * Uncontrolled systemic arterial hypertension (at rest \>150 mmHg systolic or 95 mmHg diastolic) * Uncontrolled ventricular arrhythmias * Uncontrolled bradycardia or tachycardia supraventricular arrhythmias * Myocardial infarction within the last 12 months * Pulmonary embolism within the last 12 months * Relevant changes in hemodynamic therapy or major surgery within the last 12 weeks * Musculoskeletal or peripheral vessel disorders which complicates an ergometry

Design outcomes

Primary

MeasureTime frameDescription
systolic pulmonary pressure at 50 W3-5 yearschange of systolic pulmonary arterial pressure after 3-5 years

Secondary

MeasureTime frameDescription
peak (oxygen uptake) VO23-5 yearschange of peak VO2 after 3-5 years

Countries

Austria

Outcome results

None listed

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