Houston, TXNCT02622542Now EnrollingIRB Ready

Distal Aortic Dissection Clinical Trial in Houston, TX

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

Sponsored by The University of Texas Health Science Center, Houston

Quick Self-Assessment

See if you qualify for this Houston location

Preparing your pre-screening questions…

Expert Care in Houston

Access distal aortic dissection specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related distal aortic dissection treatment provided free

Apply for This Houston Location

Check if you qualify for this distal aortic dissection clinical trial in Houston, TX

Secure & Confidential

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 Distal Aortic Dissection Study in Houston

The purpose of the study is to conduct a randomized controlled trial comparing best medical therapy (BMT) alone to BMT with thoracic endovascular aortic repair (BMT+TEVAR) for uncomplicated acute type B aortic dissection.

Sponsor: The University of Texas Health Science Center, Houston

Who Can Participate

Inclusion Criteria

Aged ≥18 years, regardless of race or ethnicity;
Diagnosed with uncomplicated ABAD, i.e., a primary entry tear distal to left subclavian artery with no evidence of malperfusion, end-organ ischemia, rupture, or intractable pain, and onset of symptoms is ≤30 days prior to enrollment;
Patient has been stabilized after the acute event with control of pain and blood pressure using ≤3 intravenous antihypertensive medications;
Adequate imaging, e.g., CT with contrast (chest + abdomen+ pelvis) is available prior to enrollment; and
Indicates willingness to comply with the study protocol and is able to provide a written informed consent;
Meets criteria for inclusion in the National Death Index and Social Security Death Master File.

Exclusion Criteria

Diagnosed with Type A aortic dissection;
Evidence of complicated ABAD;
Chronic Type B aortic dissection (\>6 weeks from onset of symptoms);
Unable to be randomized and undergo treatment according to protocol within 30 days of symptom onset;
Diagnosed with traumatic dissection or penetrating ulcer;
Anatomy is not suitable for TEVAR;
Previous descending thoracic or abdominal aortic surgery (open or endovascular);
Unsuitable access sites, including infection at access sites;
Associated aortic aneurysm (descending aortic diameter ≥5.0 cm);
Life expectancy \<2 years;
Unable or unlikely to comply with BMT;
Unable or refuse to comply with follow-up;
Intend to participate in another trial within 3 months of enrollment;
Pregnant or breast-feeding;
Vasculitis or known genetic connective tissue disorder (Marfan's syndrome or Ehlers-Danlos syndrome)
Active systemic infection;
Chronic kidney disease stage 3-5 (estimated glomerular filtration rate \<60 mL/min/1.73m2);
Cerebral vascular accident within past 3 months; or
Clinically significant gastrointestinal bleeding, major surgery, myocardial infarction, or untreated coagulopathy within past 6 weeks.

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 (NCT02622542) 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.

Distal Aortic Dissection Treatment Options in Houston, TX

If you're searching for distal aortic dissection treatment options in Houston, TX, this clinical trial (NCT02622542) 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 distal aortic dissection 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 distal aortic dissection clinical trials near you to find additional studies recruiting in your area.

More Aortic Aneurysm Trials in Houston, TX

See all aortic aneurysm clinical trials recruiting in Houston — not just this study.

Browse Aortic Aneurysm Trials in Houston →

Browse More Trials by Condition

Aortic Aneurysm TrialsInterstitial Cystitis TrialsAll Conditions →

Ready to Join in Houston?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Houston, TX