# Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy

> **NCT01792960** · — · COMPLETED · sponsor: **Yonsei University** · enrollment: 99 (actual)

## Conditions studied

- Familial Hypertrophic Cardiomyopathy

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT01792960
- **Lead sponsor:** Yonsei University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2013-02
- **Primary completion:** 2013-08
- **Final completion:** 2013-08
- **Target enrollment:** 99 (ACTUAL)
- **Last updated:** 2014-02-19


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01792960

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01792960, "Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy". Retrieved via AI Analytics 2026-06-23 from https://api.ai-analytics.org/clinical/NCT01792960. Licensed CC0.

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