Oklahoma City, OKNCT06813820Now EnrollingIRB Ready

Left Ventricle Remodeling Clinical Trial in Oklahoma City, OK

Access cutting-edge left ventricle remodeling treatment through this clinical trial at a research site in Oklahoma City. Study-provided care at no cost to qualified participants.

Sponsored by BioVentrix

Quick Self-Assessment

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Expert Care in Oklahoma City

Access left ventricle remodeling specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related left ventricle remodeling treatment provided free

Apply for This Oklahoma City Location

Check if you qualify for this left ventricle remodeling clinical trial in Oklahoma City, OK

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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 Oklahoma City

    Convenient for OK 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 Oklahoma City site if eligible
  4. 4Begin participation

About This Left Ventricle Remodeling Study in Oklahoma City

A prospective, multi-center randomized trial comparing the Revivent System plus GDMT to GDMT alone. A total of approximately 135 subjects will be randomized in a 2:1 allocation ratio (90 treatment and 45 control), with approximately 128 evaluable patients and assuming 5% loss to follow-up. A primary safety endpoint will be evaluated at 30 days. Primary efficacy endpoint will be at 1 year. Interim efficacy endpoints will be evaluated at 6 months.

Sponsor: BioVentrix

Who Can Participate

Inclusion Criteria

18 years old or older
LV Aneurysm or Scar Presence: Defined by presence of a contiguous acontractile (akinetic and/or dyskinetic) non-calcified scar
LV Aneurysm/Scar Location: Defined as a scar involving anterior, apical or anterolateral ± septal regions of the left ventricle as evidenced by cardiac imaging (Viability of myocardium in regions remote from area of intended scar

Exclusion Criteria

as evidenced by cardiac imaging)
Left Ventricular Ejection Fraction \< 40%
Left ventricular end-systolic volume index ≥60 mL/m2
Suffering from heart failure symptoms as defined by NYHA Classification \> 2 not responsive to medical therapy
Patient completed 6 Minute Walk Test and KCCQ Quality of Life Questionnaire (can be performed at baseline visit)
Patient is on adequate Guideline Directed Medical Therapy (GDMT)
Subject or a legally authorized representative must provide written informed consent
Agree to required follow-up visits
Female subject of childbearing potential does not plan pregnancy for at least one year following the index procedure. For a female of childbearing potential, a pregnancy test must be performed with negative results known within seven days prior to index procedure Exclusion Criteria: Candidates will be excluded from the study if ANY of the following conditions is present:
Cardiac Resynchronization Therapy (CRT) or ICD pacing lead placement ≤ 90 days prior to enrollment
Valvular heart disease, which in the opinion of the investigator, will require intervention (transcatheter or surgical)
Mitral Regurgitation greater than moderate (\>2+)
Need for coronary revascularization, in the opinion of the investigator
Peak Systolic Pulmonary Arterial Pressure \> 70 mm Hg via echo or right heart catheterization
Myocardial Infarction within 90 days prior to enrollment
Within the last six months, a prior CVA or TIA, or intracranial hemorrhage
Co-morbid disease process with life expectancy of less than one year or active malignancy not in remission
Severe pulmonary disease that would preclude general anesthesia
Any solid organ transplant or is on waiting list for any solid organ transplant other than cardiac
Chronic renal failure with a GFR\<30ml/min
Subject is currently participating in another clinical trial that has not yet completed its primary endpoint

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 Oklahoma City?

Yes, this clinical trial (NCT06813820) has an active research site in Oklahoma City, OK 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.

Left Ventricle Remodeling Treatment Options in Oklahoma City, OK

If you're searching for left ventricle remodeling treatment options in Oklahoma City, OK, this clinical trial (NCT06813820) 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 Oklahoma City research site is actively enrolling participants for this clinical trial. You'll receive care from experienced left ventricle remodeling 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 left ventricle remodeling clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Oklahoma City, OK