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Observational Study of Patients Undergoing Diagnostic Right Heart Catheterization
RECRUITINGSponsored by HemoCept Inc.
Actively Recruiting
SponsorHemoCept Inc.
Started2025-12-01
Est. completion2026-03-06
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT07224906
Summary
The objective of this observational pilot study is to collect HemoCept device data from subjects undergoing diagnostic right heart catheterization (RHC) procedures.
Eligibility
Age: 18 Years+Healthy volunteers accepted
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.
Conditions4
Congestive Heart Failure(CHF)Heart DiseasePulmonary HypertensionValve Disease, Heart
Locations1 site
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
SponsorHemoCept Inc.
Started2025-12-01
Est. completion2026-03-06
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT07224906