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Not yet recruiting NCT06272318

Vital Signs Blood Pressure Trial

— Observational Cardiovascular Diseases Hypertension Blood Pressure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood Pressure Cuff, EKG, PPG.
Who it may be relevant to
Registry conditions: Cardiovascular Diseases, Hypertension, Blood Pressure. Basic parameters: 18 years — 64 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this study is collect subject vitals with a blood pressure cuff, electrocardiogram (ECG), and photoplethysmogram (PPG). This data can then be used to develop a reliable, accurate, noninvasive, and continuous blood pressure monitoring device.

Interventions

  • Other Blood Pressure Cuff, EKG, PPG
    A blood pressure cuff, an EKG, and a PPG will be utilized to collect subject vitals.

Primary outcome measures

  • Collection of Subject Name (optional) [Time frame: Less than 1 minute]
  • Collection of Subject Height [Time frame: Less than 1 minute]
  • Collection of Subject Weight [Time frame: Less than 1 minute]
  • Collection of Subject Age [Time frame: Less than 1 minute]
  • Collection of Subject Medical Comorbidities [Time frame: 1 minute]
  • Systolic and Diastolic Blood Pressure Measurement [Time frame: 1-2 minutes]
  • Collection of ECG Waveforms [Time frame: 5 minutes]
  • Collection of PPG Waveforms [Time frame: 5 minutes]

Eligibility criteria

Inclusion criteria

  • Age >17 and <65 years
  • BMI >20 and <35

Exclusion criteria

  • Age <18 or >64
  • BMI <20 or >35
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06272318 · 74131

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗