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Avicena LVDP Validation Study in Healthy Volunteers

A

Avicena

Status

Completed

Conditions

Healthy

Treatments

Diagnostic Test: Non-Invasive Estimation of Left Ventricular Diastolic Pressure

Study type

Observational

Funder types

Industry

Identifiers

NCT05673174
CP-0006

Details and patient eligibility

About

The purpose of this study is to document the utility of the Vivio System in quantifying LVDP in healthy volunteers.

Enrollment

321 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Adult subjects >21 years of age.
  2. No known significant health problems.
  3. Willing and able to participate in all study evaluations.
  4. Ability to understand and sign informed consent.

Exclusion criteria

  1. Open skin lesions at the site of Vivio application / examination.
  2. Inability to obtain brachial artery blood pressure.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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