No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
300 (estimated)
Sponsor
University of Kansas Medical Center · Other
Who this trial is looking for
This trial is looking for patients with pulmonary hypertension. Participants will help create a registry to better understand the disease.
Are You a Good Fit for This Trial?
You may be able to join if
I am a patient at TUKHS or agreed to participate in an approved study.
I have been diagnosed with pulmonary hypertension confirmed by tests.
I am 18 years old or older.
You may not be able to join if
I do not want to participate.
I cannot provide informed consent.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Establish a pulmonary hypertension registry and biorepository to lead towards a further understanding of the disease.
Trial Locations
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Facility
City
State
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Status
Eligibility Criteria
Inclusion Criteria:
1. The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP)
2. The participant has a diagnosis of pulmonary hypertension confirmed by right heart catheterization
3. Patient is ≥ 18 years of age or…
Inclusion Criteria:
1. The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP)
2. The participant has a diagnosis of pulmonary hypertension confirmed by right heart catheterization
3. Patient is ≥ 18 years of age or older
Exclusion Criteria:
1. Participant declines to participate (living patients only)
2. Participant is unable to provide informed consent (living patients only)
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