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CompletedNCT01481298Updated Nov 29, 2011

Value of Cardiac Magnetic Resonance (CMR) Derived Parameters for Diagnosing Left Ventricular Non-compaction Cardiomyopathy

An observational study in Left Ventricular Non-compaction Cardiomyopathy, Left Ventricular Failure and Left Ventricular Hypertrophy, sponsored by University of Leipzig. Completed at 1 site in Germany. Open to participants aged 14 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-11-29.

Sponsored by University of Leipzig · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
57
Ages
14 Years to 64 Years
Sex
All
01

Study summary

Left ventricular non-compaction (LVNC) is a rare cardiomyopathy characterized by numerous excessively prominent left ventricular (LV) trabeculation and deep intertrabecular recesses communicating with the ventricular cavity and severely altering myocardial structure. Although most authors assume a developmental arrest in embryogenesis as the underlying pathology, the mechanisms of LVNC are not fully understood yet. Several gene mutations have been identified to be linked with LVNC and an autosomal dominant inheritance pattern is frequent To date the most commonly used imaging tool for diagnosing LVNC is echocardiography applying the criteria established by Jenni and coauthors However, qualitative parameters to differentiate normal compaction of the myocardium in healthy subjects from LVNC or from other cardiomyopathies like dilative cardiomyopathy (DCM) or hypertrophic cardiomyopathy (HCM) may fail due to highly variable LV trabeculation. Therefore, absolute quantification should be performed. Cardiac magnetic resonance (CMR) has been reported as a promising imaging modality to characterize patients with LVNC as it provides both a high spatial resolution and a good contrast between trabeculation and blood pool Jacquier et al. recently described a value of trabeculated LV myocardial mass above 20% of the global mass of the LV to be highly sensitive and specific for LVNC However, in their approach, a substantial degree of the LV cavity was included into calculated trabecular LV mass and led to systemic overestimation of the latter. Furthermore, the role and prognostic value of myocardial scarring as assessed by delayed enhancement (DE) CMR was not evaluated.

The aim of the retrospective study was to establish revised and extended CMR criteria to distinguish LVNC from DCM, HCM and a group of healthy controls and to improve the assessment of trabeculated mass by excluding intertrabecular blood pool.

02

Conditions studied

  • Left Ventricular Non-compaction Cardiomyopathy
  • Left Ventricular Failure
  • Left Ventricular Hypertrophy
03

In context

Cardiomyopathies

1,176 studies on the registry are indexed under Cardiomyopathies; 287 are open to participants now.

This study's enrollment of 57 is below the median of 153 across 515 observational studies indexed under Cardiomyopathies.

Browse Cardiomyopathies studies →

Lead sponsor

University of Leipzig is the lead sponsor of 147 studies on the registry; 24 are open to participants now.

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

04

Who can participate

Ages eligible
14 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Twelve patients (3 male, 27%) with proven LVNC, two with familial LVNC, were included into the study. The patients initially presented with symptoms of heart failure and were referred to the department of cardiology for further evaluation. All patients underwent echocardiography performed by experienced specialists and fulfilled the LVNC criteria of Jenni. CMR imaging was performed within 3 days after echocardiography. Exclusion criteria were co-existing cardiac anomalies and usual CMR contraindications such as implanted defibrillators/pacemakers. The investigators furthermore included 10 consecutive patients (4 male, 36%) with HCM and 11 consecutive patients (3 male, 27%) with DCM. The diagnosis of HCM and DCM was established according to current guidelines Patient parameters were compared to a control group of 25 healthy age matched volunteers (12 male, 48%) without history of cardiovascular disease and without clinical symptoms.

Inclusion criteria

  • left ventricular non-compaction cardiomyopathy
  • dilatative cardiomyopathy
  • hypertrophic cardiomyopathy or healty controls

Exclusion criteria

Exclusion Criteria:

  • contraindications for magnetic resonance imaging like pacemakers or other metallic implants
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
57 participants (actual)

Groups and cohorts

  • LVNC

    12 patients with left ventricular non-compaction cardiomyopathy

  • HCM

    10 patients with hypertrophic cardiomyopathy

  • DCM

    11 patients with dilatative cardiomyopathy

  • controls

    24 healthy controls

06

Study locations

1 site
  • University of Leipzig - Heart Center
    Leipzig, 04289, Germany
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT01481298
Lead sponsor
University of Leipzig
Responsible party
Matthias Grothoff, M.D. (Dr. med., University of Leipzig) — Principal investigator
First posted
Nov 29, 2011
Start date
Dec 2004
Primary completion
Jul 2008
Completion
Oct 2008
Last update
Nov 29, 2011

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2011. You cannot join it, but the record below documents what was studied.

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