New York, NYNCT04559425Now EnrollingIRB Ready

Heart Block Complete Clinical Trial in New York, NY

Access cutting-edge heart block complete treatment through this clinical trial at a research site in New York. Study-provided care at no cost to qualified participants.

Sponsored by The Hospital for Sick Children

Quick Self-Assessment

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Expert Care in New York

Access heart block complete specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related heart block complete treatment provided free

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Check if you qualify for this heart block complete clinical trial in New York, NY

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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 New York

    Convenient for NY 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 New York site if eligible
  4. 4Begin participation

About This Heart Block Complete Study in New York

Few studies are specifically designed to address health concerns that are already relevant during pregnancy. The consequence is a lack of evidence on best clinical practice. This includes mothers and their babies when pregnancy is complicated by an abnormally slow heart rate due to maternal antibody-mediated heart disease in the unborn baby (fetus). Since the late seventies, it has been possible to detect and monitor fetal disease by ultrasound images and to treat selected conditions with pharmaceuticals administered via the mother. To this day, physicians need to make decisions about the management of such pregnancies without evidence from prospective clinical trials on drug efficacy and safety. The SLOW HEART REGISTRY is a multi-centered prospective observational study that will address the knowledge gap to guide future management of high-degree immune-mediated heart block to the best of care. The study seeks to establish an international database of the management and outcome of affected fetuses, to be used to publish information on the results of currently available prenatal care and to evaluate the need for additional research.

Sponsor: The Hospital for Sick Children

Who Can Participate

Inclusion Criteria

Written informed maternal consent to participate in the Slow Heart Registry
High-degree (2nd; 2:1; 2nd-3rd or 3rd degree) AVB diagnosed ≤ 32+0 weeks with or without hydrops
Enrollment within maximally 8 days of high-degree AVB diagnosis
Positive or pending anti-Ro/La antibody test results at the time of enrollment

Exclusion Criteria

AVB associated with major CHD (e.g. left atrial isomerism, cc-TGA)
AVB with known negative anti-Ro and/or La antibody test result at enrollment
1st degree AVB
Sinus bradycardia with normal 1:1 AV conduction
Blocked atrial bigeminy (irregular atrial rate with failure of AV conduction of the premature atrial beat)
Primary delivery for postnatal treatment
Maternal-fetal conditions (other than cardiac NL) associated with high odds of premature delivery or death (e.g. renal failure, significant infectious diseases, major extracardiac anomalies, PROM, etc.)
Preexisting maternal mental disorder (e.g. bipolar, mania, severe depression, substance abuse)
Poorly controlled insulin-dependent diabetes (HbA1c \>7%) at CAVB diagnosis
Oligohydramnios (deepest/maximal vertical pocket \<2 cm)
Severe IUGR (estimated fetal weight \<3rd percentile)

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 New York?

Yes, this clinical trial (NCT04559425) has an active research site in New York, NY 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 Block Complete Treatment Options in New York, NY

If you're searching for heart block complete treatment options in New York, NY, this clinical trial (NCT04559425) 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 New York research site is actively enrolling participants for this clinical trial. You'll receive care from experienced heart block complete 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 block complete clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · New York, NY