CClinicalTrials.gg
RecruitingNCT03821051Updated Jan 29, 2019

China Structural Ventricular Arrhythmias Registry

An observational study in Ventricular Arrythmia, sponsored by China National Center for Cardiovascular Diseases. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2019-01-29.

Sponsored by China National Center for Cardiovascular Diseases · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2022, 3 years 11 months ago, but the record still lists the study as recruiting.
  • Started Oct 2017; still recruiting 8 years 11 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Sex
All
01

Study summary

This is an observational, prospective, multi-center registry ,aiming at building a risk stratification for malignant structural ventricular arrhythmias. 2000 participants will be recruited from 10 centers in China,with clinical data to be abstracted from medical records ,and blood samples to be collected for finding promising risk indicators.The follow-up should be made every 6 mouths.

Read the detailed description

In China, the prevalence and risk factors of malignant ventricular arrhythmias remain unclear. In addition ,the mainstream treatment relies on implantable devices and medication.China Malignant Ventricular Arrhythmias Study is a nation-wide complex consisting of several interrelated studies, with the aim of building a risk stratification as well as a efficient and economic strategy for early prevention and treatment.

Structural Ventricular Arrhythmias Registry, as a part of China Malignant Ventricular Arrhythmias Study, is an observational, prospective, multi-center registry, aiming at building a risk stratification for malignant structural ventricular arrhythmias. 2000 patients with definitive diagnosis will be recruited consecutively from 10 major arrhythmia centers distributed in 6 areas in China. At study entry, participants will be interviewed and asked to sign the informed consent. Demographic characteristics, medical history, clinical features, laboratory tests, imaging pictures, medications, procedures, and in-hospital outcomes of patients will be abstracted from medical records by well trained staffs .At the same time, blood samples will be collected to detect biological markers, like genes, inflammatory factors ,etc. Once enrolled, the participants will receive follow up every 6 mouths about condition of arrhythmia, medication, clinical events, etc.

02

Conditions studied

  • Ventricular Arrythmia

Browse trials for

Keywords

  • structural ventricular arrythmia
  • ischemic cardiomyopathy
  • arrhythmogenic right ventricular cardiomyopathy
  • dilated cardiomyopathy
  • hypertrophic cardiomyopathy
  • risk stratification
03

In context

Arrhythmias, Cardiac

885 studies on the registry are indexed under Arrhythmias, Cardiac; 235 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 200 across 414 observational studies indexed under Arrhythmias, Cardiac.

Browse Arrhythmias, Cardiac studies →

Lead sponsor

China National Center for Cardiovascular Diseases is the lead sponsor of 256 studies on the registry; 134 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

In 10 major arrhythmia centers distributed in 6 areas in China, 2000 patients satisfying the inclusion criteria will be enrolled consecutively.

Inclusion criteria

  • diagnosed as ventricular arrhythmia resulted by structural heart diseases, including ischemic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, dilated cardiomyopathy, hypertrophic cardiomyopathy, etc.

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. sustained tachycardia/ ventricular fibrillation or sudden cardiac death

    event of sustained ventricular tachycardia/ ventricular fibrillation or sudden cardiac death

    Time frame: 5 years

Secondary outcomes

  1. episodes of arrhythmia

    record: type of arrhythmia, the amount of episodes, duration, unstable hemodynamics,treatment,

    Time frame: 5 years

  2. all-cause death

    exclude accidents, like trauma, drowning.

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
  • China National Center for Cardiovascular Diseases
    Beijing, Beijing 100037, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03821051
Lead sponsor
China National Center for Cardiovascular Diseases
Collaborators
Renmin Hospital of Wuhan University, The First Affiliated Hospital with Nanjing Medical University, Second Affiliated Hospital of Nanchang University, Sir Run Run Shaw Hospital, West China Hospital, Beijing Anzhen Hospital, General Hospital of Shenyang Military Region, Xuzhou Central Hospital, First Affiliated Hospital, Sun Yat-Sen University
Responsible party
Sponsor
First posted
Jan 29, 2019
Start date
Oct 24, 2017
Primary completion
Oct 24, 2022 (estimated)
Completion
Oct 24, 2027 (estimated)
Last update
Jan 29, 2019

Study contacts

Yan Yao, MD,PhD
Contact
ianyao@263.net.cn
+86-13901121319
Shangyu Liu, MD
Contact
liushangyu_yu_fw@163.com
+86-18800161355
Yan Yao, MD,PhD
study chair · China National Center for Cardiovascular Diseases

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion