Temple, TXNCT04149743Now EnrollingIRB Ready

Heart Failure (HF) Clinical Trial in Temple, TX

Access cutting-edge heart failure (hf) treatment through this clinical trial at a research site in Temple. Study-provided care at no cost to qualified participants.

Sponsored by Aventusoft, LLC.

Quick Self-Assessment

See if you qualify for this Temple location

Preparing your pre-screening questions…

Expert Care in Temple

Access heart failure (hf) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related heart failure (hf) treatment provided free

Apply for This Temple Location

Check if you qualify for this heart failure (hf) clinical trial in Temple, TX

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Temple

    Convenient for TX 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 Temple site if eligible
  4. 4Begin participation

About This Heart Failure (HF) Study in Temple

Evaluation of the HEMOTAG® system in a less controlled environment and concurrently develop the system for use by patients with heart failure.

Sponsor: Aventusoft, LLC.

Who Can Participate

Inclusion Criteria

Age greater than or equal to 22 years old.
An index hospital admission for ADHF presenting with symptoms, clinical signs, and chest x-ray (CXR) findings of pulmonary congestion, receiving IV diuretics or vasoactive drugs and having a BNP \> 350 or NT-pro BNP \> 1800 pg/ml.
Able to give informed consent.
Participant's residence has adequate cellular data coverage.
Participants with previous diagnosis of left ventricular ejection fraction (LVEF) \<40% prior to the index hospitalization must have been treated for at least 90 days prior to enrollment with diuretics and beta-blocker (unless intolerant or contraindicated) and an ACE inhibitor or ARB or ARNi (unless intolerant or contraindicated).

Exclusion Criteria

Participants unable to provide informed, voluntary decision to participate in research study as determined by the investigator. (Exclude participants who necessitate the involvement of a legally authorized representative.)
Terminal condition with life expectancy less than 6 months as determined by investigator.
Participants with cardiac tamponade or constrictive pericarditis.
Participants with left ventricular assistance device (LVAD device) or had a cardiac transplantation or listed for transplantation.
Implantation of a CRT (cardiac resynchronization therapy) device during index hospitalization or intent to implant a CRT device.
Presence of hemodynamically significant mitral and/or aortic valve disease, except mitral regurgitation secondary to left ventricular dilatation, as determined by investigator.
Presence of hemodynamically significant obstructive lesions of left ventricular outflow tract, including aortic and sub-aortic stenosis, as determined by investigator.
Severe primary pulmonary, renal or hepatic disease, as determined by investigator.
Women of childbearing age (Age \<50).
History of pulmonary embolism of less than 3 months.
Dialysis dependent or dialysis initiation expected within three months.
Chronic home IV therapy or cardiac inotropes or diuretics.
Physical deformity in the chest area or lesion that may prevent proper HEMOTAG application or adjustment.
Illness/ Condition which may be aggravated or cause significant discomfort by the application of the HEMOTAG (skin issues, e.g. Intolerance to use of skin electrodes).
Impaired cognitive ability or any other state that may prevent full compliance with the study protocol, according to investigator's assessment.
Congenital heart malformations (Complex, or uncorrected congenital heart disease).
Participant enrolled in another interventional study (observational or registries are not excluded).
Participant HF is managed remotely with another monitoring device or program (for example: Pulmonary/ Lt Atrial pressure monitoring, lung fluid monitoring. BNP/pro-BNP or bioimpedance or ICD or biventricular pacemaker with impedance monitoring will be allowed unless it is part of another research protocol).
Prisoners and wards of the state.
Inability to provide informed consent (Must speak English or Spanish or Creole).

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 Temple?

Yes, this clinical trial (NCT04149743) has an active research site in Temple, TX 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.

Heart Failure (HF) Treatment Options in Temple, TX

If you're searching for heart failure (hf) treatment options in Temple, TX, this clinical trial (NCT04149743) 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 Temple research site is actively enrolling participants for this clinical trial. You'll receive care from experienced heart failure (hf) 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 heart failure (hf) clinical trials near you to find additional studies recruiting in your area.

More Heart Failure Trials in Temple, TX

See all heart failure clinical trials recruiting in Temple — not just this study.

Browse Heart Failure Trials in Temple →

Ready to Join in Temple?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Temple, TX