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3D Echo Evaluation of the Ventricles in Sclero Associated Severe PAH (EVA3D)

R

Regina Steringer-Mascherbauer

Status

Unknown

Conditions

Pulmonary Arterial Hypertension

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of the study is to document the left and right ventricular function in patients with sclerodermia associated pulmonal arterial hypertension via 3D echocardiography. The results of this study should help to generate hypothesis for further future studies.

The primary hypothesis is that the increased use of modern image guided methods could provide essential aspects for the follow up.

Full description

The 3D echocardiography could provide early and detailed information about the changes in the left and right ventricle.

The prediction of sclerodermia associated pulmonary arterial hypertension (PAH) is rather adverse, so it makes sense to evaluate relevant changes of the left-ventricular longitudinal strain soon to adapt the PAH specific therapy accordingly.

Enrollment

6 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age >17
  • pulmonary arterial hypertension (PAH) associated with WHO group 1 who start a parenteral prostanoid-therapy
  • written informed consent
  • prostanoid naive
  • no change of the PAH specific therapy within 3 weeks of the recruitment to the study

Exclusion criteria

  • pregnancy and lactation period
  • Women of child bearing potential who do not use an effective and secure method for birth control
  • severe chronic kidney insufficiency (glomerular filtration rate <30), which will remain for more than 3 months
  • liver-insufficiency Child C
  • life expectancy shorter than the course of the study (for example because of malignant disease

Trial design

6 participants in 1 patient group

no treatment

Trial contacts and locations

1

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Central trial contact

Regina Steringer-Mascherbauer, MD; Andrea Ploechl

Data sourced from clinicaltrials.gov

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