# Acquirement of Clinical and Genomic Data to Diagnose in Rare Inherited Cardiomyopathy

> **NCT06948344** · — · RECRUITING · sponsor: **Yonsei University** · enrollment: 560 (estimated)

## Conditions studied

- Cardiomyopathy
- Whole Genome Sequencing

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT06948344
- **Lead sponsor:** Yonsei University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2023-10-10
- **Primary completion:** 2028-06-30
- **Final completion:** 2028-08-22
- **Target enrollment:** 560 (ESTIMATED)
- **Last updated:** 2025-05-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06948344

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06948344, "Acquirement of Clinical and Genomic Data to Diagnose in Rare Inherited Cardiomyopathy". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06948344. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*