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Strain-area loop in drug-induced (Selexipag (Uptravi(®))) afterload reduction of the right ventricular in pulmonary arterial hypertension

Strain-area loop in drug-induced (Selexipag (Uptravi(®))) afterload reduction of the right ventricular in pulmonary arterial hypertension - SALDIAPAH

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46728
Enrollment
25
Registered
2018-05-24
Start date
2018-09-19
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

pulmonary arterial hypertension raised blood pressure in the pulmonary artery

Interventions

None listed

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - men and female patiënts, aged betweent 18 and 75 years old - PAH WHO group 1 - NYHA II-III - decision to start with Selexipag/Uptravi(®) has already been taken - legally capable, informed consent

Exclusion criteria

Exclusion criteria: - pulmonary hypertension WHO group 2-5 - other prostacyclin usage

Design outcomes

Primary

MeasureTime frame
Primary endpoints are characteristics of the strain-area loop; slope systolic deformation (Sslope), slope diastolic deformation (Dslope).

Secondary

MeasureTime frame
Secondary endpoints - occurrence of cardiovascular events and hospital admissions in the first two years after starting selexipag - characteristics of strain-area loop; intersection with the X-axis (RVEDA), intersection with the Y-axis (peakstrain)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)