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Long qt SyndromeBA-TdPNCT02439645

A Registry to Determine the Clinical and Genetic Risk Factors for Torsade De Pointes

An observational study of Long qt Syndrome and Torsade de Pointes, run by Massachusetts General Hospital at 4 sites in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

This is a registry to examine genetic and clinical predictors of torsade de pointes events. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Long qt Syndrome, Torsade de Pointes
How many people
11 participants
Where
4 sitesUnited States
Study dates
Oct 2013to 26 Jul 2019
How long will I take part?
20 Years
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Any patient in which informed consent can be obtained, with a history of torsade de points (see below designation).

Who may be able to join

  • torsade de pointes clinical syndrome according to one of the following three clinical criteria:
  • Definite TdP: At least 3 beats of polymorphic ventricular tachycardia (VT) or ventricular fibrillation (VF) on a 12-lead ECG or rhythm strip with documented QTc > 450 ms in men or QTc > 470 in women (excluding patients with conduction block or AF at baseline, see below) prior to arrhythmic event.
  • Probable TdP: At least 3 beats of polymorphic VT or VF on a 12-lead ECG or rhythm strip with QTc > 450ms (men) or 470ms (women) after the event, or polymorphic VT or VF episode not meeting criteria for 'definite TdP' but determined by the adjudicating physician to be likely TdP. For patients having a cardiac arrest, at least 1 hour after restoration of normal rhythm or after secondary hypoxia or electrolyte abnormalities have been ruled out (confounders of QT prolongation often seen post-arrest47) will be required.
  • Possible TdP: Unexplained syncope in a patient presenting with QTc > 450ms (men) or 470ms (women).

Who cannot join

  • age <18 years old
  • inability to obtain informed consent from the patient or a family member
  • no exclusion on the basis of race or gender.

Trial locations and contacts

4 sites in 1 country.

United States4 sites
  • Massachusetts General Hospital

    Boston, Massachusetts, 02114

  • Boston University Medical Center

    Boston, Massachusetts, 02118

  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215

  • West Roxbury VA Medical Center

    West Roxbury, Massachusetts, 02132

Other trials in United States

About this study

This is a registry to examine genetic and clinical predictors of torsade de pointes events.

Read the detailed description

BACKGROUND AND SIGNIFICANCE Drug-induced long QT syndrome (LQTS), and the subsequent fatal arrhythmia torsade de pointes (TdP), is an important side effect associated with the use of a number of medications. Prolongation of the QT interval is the most common cause of withdrawal of medications already on the market, and despite the relatively rarity with non-cardiovascular drugs, the public health impact is magnified by the fact that drug-induced TdP can occur with medications used for benign conditions, such as allergic rhinitis. The QT interval is heritable, and a number of common genetic variants have been associated with QT interval in large population studies.

Although common genetic variants associated with sudden cardiac death have been identified, studies specifically identifying variants associated with drug-induced LQTS and TdP are limited. Smaller studies have suggested that variants of genes associated with QT interval duration in the population in general are also associated with the risk of drug-induced QT prolongation and TdP, but larger studies are needed. Moreover, an improved ability to predict the causes of TdP requires a careful search for clinical factors associated with TdP compared to controls.

RESEARCH DESIGN AND METHODS

  1. Study Design and Enrollment: We propose to conduct a multi-center research study to examine known and explore potentially unknown genetic and clinical predictors of torsade de pointes (TdP) also known as acquired long QT syndrome (LQTS) through creation of a registry. Any patient with a documented history of a torsade de pointes (TdP) event will be eligible. Patients must be able to understand the risks of genetic testing, and be willing to undergo a venipuncture for blood collection for genotyping. Exclusion criteria include inability to provide informed consent. We plan to enroll a total of 200 study participants total across all participating centers. Massachusetts General Hospital will be the coordinating center of this multi-center study of medical institutions within the greater Boston and New England area. In a substudy to take place at MGH, subjects will be invited to have a punch biopsy of the skin to allow creation of inducible pluripotent stem cells that can be differentiated into cardiomyocytes for further characterization of the repolarization phenotype.
  2. Study Procedures: We will screen patients for enrollment including both retrospective (event prior to the start of the study) and prospective (event following the start of the study) components. Patients will be identified by investigators based on clinical characteristics, and following explanation of the study by co-investigators, will be asked about participation either during routine scheduled follow-up (for retrospective cases) or at the sentinel event. Investigators will complete a data collection form for each patient, which will include contact information, demographic information, clinical information, family history and pedigree, and all electrocardiography information available (12-lead ECGs, rhythm strips and summary reports). No information about mental illness will be collected. Patients will then undergo venipuncture, and four 5mL blood samples will be collected for genotyping and plasma analysis. For patients who are willing, a 3mm punch biopsy from the shoulder, upper thigh, small of the back, or buttock (subject's choice) will be obtained for fibroblast culture. Patients who are recruited at non-MGH sites will have a visit to MGH scheduled in order to obtain the skin biopsy. Induced pluripotent stem cells will be made from the fibroblast cultures and differentiated to cardiomyocytes in order to assess the cellular phenotype. Patients will also be consented for future re-contact about additional data, information, or samples needed for analysis. All clinical information and samples (including DNA and blood) collected at participating centers will be transferred to Dr. Newton-Cheh at MGH for storage and analysis.
Keywords
genetic research
Medical subject headings
Long QT Syndrome, Torsades de Pointes

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Torsade de pointes arrhythmia events

    1. Definite TdP: At least 3 beats of polymorphic ventricular tachycardia (VT) or ventricular fibrillation (VF) on a 12-lead ECG or rhythm strip with documented QTc > 450 ms in men or QTc > 470 in women (excluding patients with conduction block or AF at baseline, see below) prior to arrhythmic event.
    2. Probable TdP: At least 3 beats of polymorphic VT or VF on a 12-lead ECG or rhythm strip with QTc > 450ms (men) or 470ms (women) after the event, or polymorphic VT or VF episode not meeting criteria for 'definite TdP' but determined by the adjudicating physician to be likely TdP. For patients having a cardiac arrest, at least 1 hour after restoration of normal rhythm or after secondary hypoxia or electrolyte abnormalities have been ruled out (confounders of QT prolongation often seen post-arrest47) will be required.
    3. Possible TdP: Unexplained syncope in a patient presenting with QTc > 450ms (men) or 470ms (women).

    Measured: Participants will be followed for the time to obtain consent, clinical information and biospecimens (typically < 1 day)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 May 2015 (estimated)
  2. Study startOct 2013
  3. Primary completion26 Jul 2019
  4. Study completion26 Jul 2019

Why it stopped: Study was terminated lack of recruitment, small number of eligible cases (11 enrolled, 1 found ineligible after enrollment), unlikely to be able to achieve study goals due to low recruitment.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
11 participants (actual)
Target duration
20 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT02439645
Sponsor's protocol ID
2013P001531
Acronym
BA-TdP
Status last verified
Nov 2021
First submitted
5 May 2015
Last updated
3 Dec 2021
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Long qt Syndrome and Torsade de Pointes, run by Massachusetts General Hospital at 4 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 3 Dec 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Study was terminated lack of recruitment, small number of eligible cases (11 enrolled, 1 found ineligible after enrollment), unlikely to be able to achieve study goals due to low recruitment.). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Torsade de pointes arrhythmia events (time frame: Participants will be followed for the time to obtain consent, clinical information and biospecimens (typically < 1 day)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Dec 2021.

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