No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Diagnostic
Participants needed
20 (estimated)
Sponsor
Bastiaan Driehuys · Other
Who this trial is looking for
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The overall study objectives outlined in this study are to derive 129Xe MRI pulmonary vascular biomarker signatures that differentiate common subtypes of PAH and to determine the ability of 129Xe MRI to longitudinally monitor disease progression and response to therapy in PAH, with the aid of additional assessments, such as labs, echocardiography, and six-minute walk distance (6MWD).
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
Arm 1 -IPAH
* Age: 18-75 years
* WHO functional class 2 or 3
* Mean pulmonary artery pressures \> 20 mmHg
* Pulmonary capillary wedge pressure ≤15 mmHg
* Pulmonary vascular resistance \> 2 Wood Units (WU)
* No other cause identified for PAH
Arm 2 -PAH-CTD
* Age: 18-75 years
*…
Inclusion Criteria:
Arm 1 -IPAH
* Age: 18-75 years
* WHO functional class 2 or 3
* Mean pulmonary artery pressures \> 20 mmHg
* Pulmonary capillary wedge pressure ≤15 mmHg
* Pulmonary vascular resistance \> 2 Wood Units (WU)
* No other cause identified for PAH
Arm 2 -PAH-CTD
* Age: 18-75 years
* WHO functional class (FC) 2 or 3
* Mean pulmonary artery pressures \> 20 mmHg
* Pulmonary capillary wedge pressure ≤15 mmHg
* Pulmonary vascular resistance \> 2 WU
* Diagnosis of connective tissue disease
Exclusion Criteria:
* PH other than Idiopathic PAH or PAH associated with CTD; any conditions that prevent the performance of 129Xe MRI scans will be excluded from the study.
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