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An Evaluation Of The Novel TRAMINER Sequence By Comparison To Late Gadolinium Enhancement Images

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Myocardial Fibrosis
Cardiovascular Disease

Treatments

Other: Traminer MRI Sequence

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02727725
AHC IRB 5886

Details and patient eligibility

About

  • The purpose of this study is to show that the novel TRAMINER (T(Rho) and Magnetization Transfer and Inversion Recovery) sequence provides at least as good visualization and detection of sub-endocardial scarring, fibrosis, and acute infarction as the current gold standard Inversion Recovery (IR) Turbo-Flash sequence.
  • The hypothesis is that the TRAMINER sequence has the same or higher sensitivity in detecting small sub-endocardial scarring than the inversion recovery segmented gradient echo sequence known as IR-Turbo Fast low angle shot (IR Turbo-Flash), which is the accepted current gold standard for the detection of myocardial viability.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults ≥18 years of age referred for a cardiac MRI with Gadolinium enhancement only at Advocate Lutheran General Hospital

Exclusion criteria

  • <18 years old,
  • Adults unable to consent
  • Adults for whom the MRI has not been previously scheduled
  • Adults with an order for any MRI other than cardiac MRI with Gadolinium enhancement

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Traminer MRI Sequence
Experimental group
Description:
The TRAMINER MRI sequence implementation to be tested allows the acquisition of high resolution MR images in the free-breathing patient, by combining multiple averages and motion correction with the TRAMINER preparation.
Treatment:
Other: Traminer MRI Sequence

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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