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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02727725
Other study ID # AHC IRB 5886
Secondary ID
Status Completed
Phase N/A
First received February 24, 2016
Last updated March 13, 2018
Start date January 15, 2016
Est. completion date January 15, 2018

Study information

Verified date March 2018
Source Advocate Health Care
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

- 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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 15, 2018
Est. primary completion date January 15, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Other:
Traminer MRI Sequence
The Traminer MRI sequence will be added to the standard IR Turbo-Flash sequence and last 2-5 minutes.

Locations

Country Name City State
United States Advocate Lutheran General Hospital Park Ridge Illinois

Sponsors (2)

Lead Sponsor Collaborator
Advocate Health Care Siemens Corporation, Corporate Technology

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity of the TRAMINER sequence in detecting myocardial fibrosis or acute infarction compared to the gold standard sequence will be measured. The method of assessment is through a score using the 17 segment model of myocardial map. 6-12 months
Secondary Reduction in clinical Magnetic Resonance (MRI) procedure time. 6-12 months
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