RECRUITING

VicorderCS NIBP Validation Study to Review The Ability to Capture Blood Pressure Measurements

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

80 Beats Medical introduces the VicorderCS, the next generation of our Vicorder technology designed to manage hypertension and cardiovascular risks. This advanced diagnostic equipment offers non-invasive collection and computation of a plethora of cardiovascular markers. It is faster, easier to use, and more portable than its predecessor, with enhanced connectivity options for extended marker collection and analysis. These markers enable early diagnosis of cardiovascular disease, ensuring positive patient outcomes. With a strong foundation in numerous published clinical studies, the VicorderCS enhances data collection and analysis capabilities, empowering the research community in developing new drugs and therapeutics. This validation study is purposed to evaluate one of the physiological parameters that is measured by the VicorderCS system, which is Non-invasive Blood Pressure (NIBP) via the common oscillometric cuff-based method.

Official Title

VicorderCS NIBP Validation Study to Assess Its Ability to Capture Blood Pressure Measurements

Quick Facts

Study Start:2024-08-15
Study Completion:2025-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06560034

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Any gender, in good general health
  2. * Must be 18 years old or older, inclusive at enrollment
  3. * Must be willing to provide blood pressure measurement
  4. * Must be able to read, understand, and willingly sign an Informed Consent Form
  5. * Must be able to read, speak and understand English
  6. * Must be available to attend one study visit at: please specify exact location.
  1. * Excluding subjects with significantly irregular heart rhythm (e.g. Bigeminy, trigeminy, isolated ventricular premature beat (VPB), atrial fibrillation) or are pregnant
  2. * No active email address
  3. * Non-English or Spanish- speaking
  4. * Unable to read in English.

Contacts and Locations

Study Contact

Nitin Vaswani, MD
CONTACT
2025396941
nitin@manoshealth.com
Brian Van Winkle, MBA
CONTACT
2025396941
brian@manoshealth.com

Principal Investigator

Nitin Vaswani, MD
PRINCIPAL_INVESTIGATOR
PI

Study Locations (Sites)

Manos Health Study Site
Breckenridge, Colorado, 80424
United States

Collaborators and Investigators

Sponsor: 80 Beats Medical

  • Nitin Vaswani, MD, PRINCIPAL_INVESTIGATOR, PI

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-15
Study Completion Date2025-08-01

Study Record Updates

Study Start Date2024-08-15
Study Completion Date2025-08-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cardiovascular Diseases
  • Blood Pressure
  • Hypertension