Broomfield, CONCT07507903Now EnrollingIRB Ready

Hypertension Clinical Trial in Broomfield, CO

Access cutting-edge hypertension treatment through this clinical trial at a research site in Broomfield. Study-provided care at no cost to qualified participants.

Sponsored by Aktiia SA

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Expert Care in Broomfield

Access hypertension specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related hypertension treatment provided free

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Check if you qualify for this hypertension clinical trial in Broomfield, CO

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Broomfield

    Convenient for CO residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Broomfield site if eligible
  4. 4Begin participation

About This Hypertension Study in Broomfield

This study, with N = 85 participants minimum over 3 visits spread over 7 days, has been designed to assess the accuracy and precision of the Blood Pressure and pulse rate values as generated by Aktiia.product-G1-US for up to 7 days after initialization in a cohort of subjects representative of the US population.

Sponsor: Aktiia SA

Who Can Participate

Inclusion Criteria

Participants must be able to provide informed consent to participate.
Participants must be willing and able to comply with all of the study procedures and return for a second visit one week later.
Participants must be 22 to 59 years of age.
Participants or witnesses must be able to read or write in English.

Exclusion Criteria

Participants with compromised circulation, injury, or physical malformation of the equipment test sites or other sensor sites which would limit the ability to test sites needed for the study. (Note: Certain malformations may still allow participants to participate if the condition is noted and would not affect the sites utilized.)
Female participants who are known to be pregnant or who are trying to get pregnant confirmed by a visit 1 and, if applicable, visit 2 positive urine pregnancy test, unless the study participants are known to be not of child-bearing potential .
Participants with known history of clotting disorders or blood clots, or currently taking a prescription blood thinner.
Other known health conditions that will prevent safe participation in the study upon disclosure in Health Assessment Short Form or verbally.
Participants suffering from sporadic or sustained cardiac arrhythmias that can lead to weak or unstable pressure pulses including but not limited to tachycardia (heart rate at rest \> 120bpm) and atrial fibrillation.
Participants suffering from sporadic or sustained reduction of peripheral perfusion that can lead to weak or unstable pressure pulses including but not limited to: Raynaud's disease, diabetes (Type I and Type II), renal dysfunctions (eGFR \< 60mL / min / 1.73 m2), hyper- / hypothyroidism, pheochromocytoma, arteriovenous fistula, and valvular heart diseases.
A wrist circumference below 14 cm or above 23 cm.
An upper-arm circumference \<22 cm or \> 42cm.
Any subject that, in the opinion of the investigator, does not exhibit any phenotype relevant to the objectives of this study.
Any condition or circumstance that, in the opinion of the investigator, may preclude study completion, interfere with accurate data collection, or bias the results, by instance a subject presenting a lateral Blood Pressure difference at screening of more than 15 mmHg for the systolic and/or more than 10 mmHg for the diastolic.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Broomfield?

Yes, this clinical trial (NCT07507903) has an active research site in Broomfield, CO that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Hypertension Treatment Options in Broomfield, CO

If you're searching for hypertension treatment options in Broomfield, CO, this clinical trial (NCT07507903) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Broomfield research site is actively enrolling participants for this clinical trial. You'll receive care from experienced hypertension specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all hypertension clinical trials near you to find additional studies recruiting in your area.

More Hypertension Trials in Broomfield, CO

See all hypertension clinical trials recruiting in Broomfield — not just this study.

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