RecruitingPhase not listed

Observational Study of Patients Undergoing Diagnostic Right Heart Catheterization

Observational Study of the HemoCept Device During Right Heart Catheterization at Boulder Heart

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This small study collects data from the HemoCept device during a right heart catheterization. This test uses a thin tube to check the right side of the heart. The study is for adults scheduled to have this test.

The objective of this observational pilot study is to collect HemoCept device data from subjects undergoing diagnostic right heart catheterization (RHC) procedures.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • You are age 18 or older. Any gender may join.
  • You or your representative must freely sign a consent form before any study steps begin.
  • You must be able and willing to agree to join and give permission to use your health information.
  • You must be able and willing to follow all study requirements.
  • You are scheduled for a right heart catheterization, either alone or with a left heart catheterization. A left-heart-only test does not qualify.

Who can't join

  • You are pregnant, breastfeeding, or plan to become pregnant during the study.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: * Subjects or representatives must have voluntarily signed the informed consent form before any study related procedures. * Subjects can be any gender but must be age 18 or older. * Subject is able and willing to provide informed consent and HIPAA authorization. * Subject is able and willing to meet all study requirements. * Scheduled for a diagnostic right heart catheterization (RHC-only or combined RHC+LHC; left-heart-only procedures are not eligible) Exclusion Criteria: * Subject is pregnant, breastfeeding, or intends to become pregnant during this study.

Study sites (1)

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