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NCT06604169Active, not recruiting

An Observational Study of Subcutaneous Implantable Cardioverter Defibrillator in Patients with Hypertrophic Cardiomyopathy At High Risk of Sudden Cardiac Death

Source: ClinicalTrials.gov · Last updated 19 Sept 2024

Brief summary (registry, in English)

1. To observe the failure rate of S-ICD screening in HCM patients at high risk of SCD. 2. To observe the incidence of IAS in HCM patients with S-ICD implantation and explore the related factors of IAS.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
589 (estimated)
First submitted
18 Sept 2024
Start date
1 Aug 2024
Primary completion date
31 Jul 2027
Lead sponsor
China National Center for Cardiovascular Diseases
NCT number
NCT06604169

What you commit to

  • Study type: Observational
  • Planned participants: 589
  • From 1 Aug 2024 to the primary completion date, 31 Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Frequent monomorphic ventricular tachycardia require ATP therapy;

Other illness

  • Combined with other diseases, life expectancy is less than 1 year.

Other

  • Combined with bradycardia with pacing indications;
  • With indications of CRT;

Who the study is looking for

  • HCM patients assessed as meeting the ICD implantation indication

Age in the registry: 14 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fuwai Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.