Health TrialsbyHealthPanel

Pulmonary Hypertension Biorepository and Registry

ConditionsPulmonary HypertensionPulmonary Arterial HypertensionPulmonary Hypertension Due to Left Heart DiseasePulmonary Hypertension, PrimaryPulmonary Hypertension Due to Lung Diseases and HypoxiaPulmonary Hypertension, Primary, 4Pulmonary Hypertension, Primary, 2Pulmonary Hypertension, Primary, 3Chronic Thromboembolic Pulmonary Hypertension
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Kansas Medical Center

About this trial

Establish a pulmonary hypertension registry and biorepository to lead towards a further understanding of the disease.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP)

The participant has a diagnosis of pulmonary hypertension confirmed by right heart catheterization

Patient is ≥ 18 years of age or older

Disqualifiers

Participant declines to participate (living patients only)

Participant is unable to provide informed consent (living patients only)

Trial population

Pulmonary Hypertension Group 1-5

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Collect Clinical Data

Collect clinically obtained data from current and deceased patients with pulmonary hypertension to support research.

Time frame
From Enrollment to 6 Months
2

Establish a Biorepository

Establish a collection of biospecimens from patients with pulmonary hypertension.

Time frame
From Enrollment to 6 Months
3

Biospecimens Collection

Correlate biospecimens to longitudinally collected individual patient data.

Time frame
From Enrollment to 12 Months
4

Collaborate

Provide biospecimens to researchers investigating pulmonary hypertension. Separate IRB approval will be needed for these studies.

Time frame
From Enrollment to 24 Months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Kansas Medical Center

Lead sponsor

Source ClinicalTrials.gov
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