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Repaired Tetralogy of Fallot: Risc Score From MRI & Clinical Data to Predict the Need for Change of Treatment

MRI in Repaired Tetralogy of Fallot: Risc Score Derived From Multiparametric Magnetic Resonance-Imaging and Clinical Data to Sharpen the Indication for Change of Individualized Treatment

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05916976
Acronym
rTOF-MR-SHARP
Enrollment
70
Registered
2023-06-23
Start date
2023-10-15
Completion date
2026-04-30
Last updated
2023-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Disease, Tetralogy of Fallot

Keywords

MRI, Tetralogy of Fallot, Multiparametric score, cardiac

Brief summary

Patient with Tetralogy of Fallot need live-long surveillance after initial operative correction (rTOF). MRI is an established and important component of the standardized follow-up in this patient population. A new score will be used to summarize the multitude of MRI-based parameters into a single number. Individual modificators are assigned to the components of the score. The value of each modificatory will be determined as a result of this feasibility trial. This new compound score is designed to anticipate any deterioration of cardiac function, arrhythmias or sudden cardiac death. This feasibility study is the first step to establish this score and find initial values for the modifies that are assigned to the more than 40 biomarkers from MRI, clinical examinations and serum parameters that are included in this new score.

Detailed description

Patient with Tetralogy of Fallot need live-long surveillance after initial operative correction (rTOF). MRI is an established and important component of the standardized follow-up in this patient population. Though a large number of diverse MRI-derived parameter have been shown to correlate with the incidence of major adverse cardiac events in patients with rTOF, there is not a single MRI-derived parameter that reliably predicts the incidence of heart failure, malignant arrhythmias or sudden cardiac death - the most common major adverse cardiac events in this group (rTOF-MACE). This feasibility trial is set to evaluate the feasibility of a weighted compound risk score based on about 40 parameters derived from MRI and augmented by clinical as well as serum-based biomarkers. This trial will recruit 70 consecutive patients with rTOF and correlate the new compound score with the clinical course over 2 years and the incidence of any change in therapy due to cardiac reasons. At the end of the trial each of the contributing parameters of the compound score will have been assigned a modifier based on its statistical relevance for the prediction of patient-specific rTOF-MACE or any change in cardiac related therapy. Based on this feasibility trial we aim to use the weighted compound score in a large multicenter trial to proof its applicability and relevance to short, medium and longterm prognosis of this special patient group.

Interventions

DIAGNOSTIC_TESTcardiac MRI

Multiparametric MRI of the heart

Sponsors

University Medical Center Goettingen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

MRI data are made available for clinical decision. Score will not be made available to treatment decision team. Nor is the study team involved in the clinical decision process until completion of follow-up data acquisition

Intervention model description

all patients scheduled for MRI for follow-up of repaired Tetralogy of Fallot.

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* rTOF; age above 16; eligible for MRI-exam

Exclusion criteria

* any contraindications to MRI; unstable patient; unresponsive patient

Design outcomes

Primary

MeasureTime frameDescription
Modified therapy cardiovascular24 monthsAny change in therapy related to cardiovascular function

Secondary

MeasureTime frameDescription
hospitalization24 monthsNeed of hospital admission due to any cardiovascular cause
cardiac intervention24 monthsAny cardiac invasive / minimal invasive intervention

Countries

Germany

Contacts

Primary ContactAnne M Weber
radiology@med.uni-goettingen.de+4955139
Backup ContactClaudia Dellas, MD
dellas@med.uni-goettingen.de+4955139

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026