Houston, TXNCT05511246Now EnrollingIRB Ready

Ventricular Tachycardia Clinical Trial in Houston, TX

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

Sponsored by The Methodist Hospital Research Institute

Quick Self-Assessment

See if you qualify for this Houston location

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Expert Care in Houston

Access ventricular tachycardia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related ventricular tachycardia treatment provided free

Apply for This Houston Location

Check if you qualify for this ventricular tachycardia clinical trial in Houston, TX

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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 Houston

    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 Houston site if eligible
  4. 4Begin participation

About This Ventricular Tachycardia Study in Houston

Comparative effectiveness randomized clinical trial, comparing endocardial radiofrequency ablation alone vs radiofrequency ablation combined with venous ethanol in patients with ischemic ventricular tachycardia -Venous Ethanol for Left Ventricular Ischemic Ventricular Tachycardia -VELVET clinical trial

Sponsor: The Methodist Hospital Research Institute

Who Can Participate

Inclusion Criteria

Male and female, ages of 18 and 85 years and with a prior ICD implant
Diagnosed with ischemic cardiomyopathy: Prior myocardial infarction (pathological Q waves or imaging evidence of regional myocardial akinesis/thinning in the absence of a non-ischemic cause)
One of the following VT events (within last 6 months): a) ≥3 episodes of VT treated with anti-tachycardia pacing (ATP) or anti-arrhythmic drugs; b) ≥1 appropriate ICD shocks; c) ≥3 VT episodes within 24 hr; d) sustained VT below detection rate of the ICD documented by EKG/cardiac monitor
Patients deemed candidates for RF ablation of VT
Able and willing to comply with pre-, post-, and follow-up requirements
Willing to sign the informed consent

Exclusion Criteria

Serum creatinine \>1.5 mg/dL, or creatinine clearance \<30 ml/min
Left ventricular (LV) ejection fraction ≤10%
Mobile LV thrombus on echocardiography
Absence of vascular access to the LV
Disease process likely to limit survival to \<12 months
New York Heart Association class IV heart failure
Cardiac surgery within the past 2 months (unless VT was incessant),
Acute coronary syndrome in the past 2 months (acute thrombus diagnosed by coronary angiography, or dynamic ST segment changes demonstrated on EKG)
Another reversible cause of VT (e.g. electrolyte abnormalities, drug-induced arrhythmia)
Severe aortic stenosis or mitral regurgitation with a flail leaflet
Unwilling or unable to provide informed consent
Covid-19 positive testing within 14 days of randomization procedure
Enrolled, or planning to get enrolled, in another research study during his/her participation on the Velvet trial

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 Houston?

Yes, this clinical trial (NCT05511246) has an active research site in Houston, 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.

Ventricular Tachycardia Treatment Options in Houston, TX

If you're searching for ventricular tachycardia treatment options in Houston, TX, this clinical trial (NCT05511246) 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 Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced ventricular tachycardia 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 ventricular tachycardia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Houston, TX