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Detecting Changes in Arterial Blood Volume and Cardiac Efficiency

Recruitingn/aAges 18 Years - 80 YearsAllHemoCept Inc.
NCT07205341 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The objective of this Pilot Study is to demonstrate the efficacy of the Hemocept device in detecting changes in arterial blood volume and cardiac efficiency.

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📋 Eligibility rules (as published)
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 between (and including) the ages of 18 and 80. * Subject ls being treated by the participating healthcare facility . ., Subject requires a trans-aortic valve replacement. * Subject is able and willing to provide informed consent and HIPM authorization. * Subject is able and willing to meet all study requirements. Exclusion Criteria: * Subject is pregnant, breast-feeding, or intends to become pregnant during the course of the study. * Subject has a personal medical history that includes: * Long O-T syndrome * Cardiac channelopathies * Seizures
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What it tests

  • Not listed
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Where

1 site
Boulder Heart
Boulder, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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