NCT06272318

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
2mo left

Started May 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress64%
May 2026Sep 2026

First Submitted

Initial submission to the registry

February 6, 2024

Completed
16 days until next milestone

First Posted

Study publicly available on registry

February 22, 2024

Completed
2.2 years until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2026

Last Updated

April 24, 2026

Status Verified

April 1, 2026

Enrollment Period

5 months

First QC Date

February 6, 2024

Last Update Submit

April 21, 2026

Conditions

HypertensionCardiovascular DiseasesBlood Pressure

Outcome Measures

Primary Outcomes (8)

  • Collection of Subject Name (optional)

    Less than 1 minute

  • Collection of Subject Height

    Height in meters

    Less than 1 minute

  • Collection of Subject Weight

    Weight in kilograms

    Less than 1 minute

  • Collection of Subject Age

    Age in years

    Less than 1 minute

  • Collection of Subject Medical Comorbidities

    1 minute

  • Systolic and Diastolic Blood Pressure Measurement

    Using blood pressure cuff; measured three times to find the initial, interim, and final blood pressure

    1-2 minutes

  • Collection of ECG Waveforms

    Using an electrocardiogram (ECG) to measure heart rhythm

    5 minutes

  • Collection of PPG Waveforms

    Using a photoplethysmography (PPG) to monitor heart rate

    5 minutes

Interventions

Blood Pressure Cuff, EKG, PPGOTHER

A blood pressure cuff, an EKG, and a PPG will be utilized to collect subject vitals.

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Participants with a range of health conditions are needed for this study, including those with cardiac or blood pressure issues, as well as individuals who are considered healthy.

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Cardiovascular DiseasesHypertension

Interventions

serglycin

Condition Hierarchy (Ancestors)

Vascular Diseases

Central Study Contacts

Ariel Clinical Research Coordinator Associate

CONTACT

650-724-3021arielkay@stanford.edu

Maya Clinical Research Coordinator Associate

CONTACT

mcaple@stanford.edu

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 6, 2024

First Posted

February 22, 2024

Study Start

May 1, 2026

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

September 30, 2026

Last Updated

April 24, 2026

Record last verified: 2026-04