# The Deep Phenotype of Lamin A/C Cardiomyopathy

> **NCT03860454** · — · UNKNOWN · sponsor: **University College, London** · enrollment: 150 (estimated)

## Conditions studied

- Lamin A/C Gene Mutation
- Dilated Cardiomyopathy, Familial

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT03860454
- **Lead sponsor:** University College, London
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-03-07
- **Primary completion:** 2025-02-01
- **Final completion:** 2025-02-01
- **Target enrollment:** 150 (ESTIMATED)
- **Last updated:** 2019-10-16

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03860454

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03860454, "The Deep Phenotype of Lamin A/C Cardiomyopathy". Retrieved via AI Analytics 2026-07-18 from https://api.ai-analytics.org/clinical/NCT03860454. Licensed CC0.

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