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Recruiting NCT07219693

NCT07219693 QuantaFlo HD Clinical Validation Study

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Clinical Trial Summary
NCT ID NCT07219693
Status Recruiting
Phase
Sponsor Semler Scientific
Condition To Assess Cardiovascular Function
Study Type OBSERVATIONAL
Enrollment 600 participants
Start Date 2025-08-21
Primary Completion 2026-03-31

Eligibility & Interventions

Sex All sexes
Min Age 22 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
QuantaFlo HD

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 600 participants in total. It began in 2025-08-21 with a primary completion date of 2026-03-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary aim of this validation protocol is to assess cardiovascular function through transthoracic echocardiography ("Echo") measurements and the QuantaFlo HD test measuring blood flow at the finger during a forced expiration ("FE"). The study examines whether Echo-measured GLS values greater than -16% correlate with abnormal responses during FE as measured by QuantaFlo HD.

Eligibility Criteria

Inclusion Criteria: * Male and female adult (≥ age 22) subjects with a minimum of 1 of the following: * A history of Cardiovascular Diseasei or PAD * Recorded history of at least two of the following * Hypertension * Diabetes * Hyperlipidemia Exclusion Criteria: * Unable to safely perform a forced expiration, or unable to obtain a technically adequate FE test result * Subjects with a pacemaker or ICD with pacemaker function * Terminal advanced illness * Recent cardiothoracic surgery (within 12 months) * Retinal eye disease with anticoagulants * History of eye surgery, within 90 days * Uncontrolled hypertension \>180 mmHg systolic pressure or \>100 mmHg diastolic pressure * Subjects with severe tremors

Contact & Investigator

Central Contact

Gena Parker

✉ gparker@semlerscientific.com

📞 669-230-2729

Frequently Asked Questions

Who can join the NCT07219693 clinical trial?

This trial is open to participants of all sexes, aged 22 Years or older, studying To Assess Cardiovascular Function. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07219693 currently recruiting?

Yes, NCT07219693 is actively recruiting participants. Contact the research team at gparker@semlerscientific.com for enrollment information.

Where is the NCT07219693 trial being conducted?

This trial is being conducted at Tucson, United States.

Who is sponsoring the NCT07219693 clinical trial?

NCT07219693 is sponsored by Semler Scientific. The trial plans to enroll 600 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology