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De klinische studie NCT06735521 (CMR_TCPC) voor Univentriculair hart, Microvasculaire disfunctie, Hartfalen, Magnetic Resonance is recruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag.
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Kaartweergave

Cardiac Magnetic Resonance Stress-perfusion Study in Patinets with Fontan Circulation (CMR_TCPC)

Recruterend
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De klinische studie NCT06735521 (CMR_TCPC) is een observationeel studie bij Univentriculair hart, Microvasculaire disfunctie, Hartfalen, Magnetic Resonance met de status recruterend. Het doel is om 30 deelnemers te includeren vanaf 15 april 2024. De studie wordt geleid door Karolinska Instituut en de voltooiing is gepland op 1 september 2025. Laatste update op ClinicalTrials.gov: 16 december 2024.
Beknopte samenvatting
Univentricular heart (UVH) is a severe congenital heart disease. Accurate advanced non-invasive diagnostic methods is limited. Cardiovascular magnetic resonance (CMR) imaging has evolved as a particularly useful tool for the study of patients with adult congenital heart disease (ACHD) considering its ability to determine detailed anatomy and detect early cardiac dysfunction without the need for radiation exposure. Most of contemporary treatment recommendations are based on consensus opinions/documents and small studies from local, or national registries. Improved knowledge is needed in all these areas to facilitate clinical decisions regarding treatment, monitoring and follow-up.

This study seeks to answer if early detection of deterioration in cardiac function, venous pressure and microvascular dysfunction can identify patients before the symptoms progress and thus help to initiate early treatment. The hypothesis is that quantitative myocardial stress-perfusion maps improves the pathophysiological insight in patients with UVH.

The overall goal with this research proposal is to implement combined advanced CMR imaging for a comprehensive non-invasive mapping of functional cardiovascular behavior in patients with complex UVH disease. The outcome of this research may benefit this young adult patient population due to early detection of cardiac disease, less hospitalizations because of heart failure, and eventually decrease morbidity and mortality.

Uitgebreide beschrijving
CMR is performed supine with a Magnetom Aera® 1.5 Tesla (T) scanner (Siemens Healthcare, Erlangen, Germany), with a phased-array 18-channel body matrix coil and a spine matrix coil. A venous blood sample is drawn to determine hematocrit and blood creatinine prior to imaging. Full coverage retrospective electrocardiographic (ECG)-gated balanced steady state free precession (bSSFP) cine imaging is acquired in standard three long-axis and short-axis slices. Typical imaging parameters are flip angle 68°, pixel size 1.4 × 1.9 mm2, slice thickness 8.0 mm, echo time (TE)/repetition time (TR) 1.19/37.05 ms, matrix size 256 × 144 and field of view (FOV) 360 × 270 mm2.

Using first-pass perfusion imaging, quantitative perfusion maps (ml/min/g) are acquired in one short-axis and one long-axis slice (mid-ventricular, 2-chamber) during administration of an intravenous contrast-agent bolus (0.05 mmol/kg, gadobutrol, Gadovist, Bayer AB, Solna, Sweden), during adenosine infusion (110 µg/kg/min or increased according to clinical routine to 140 µg/kg/min in the absence of adequate response to adenosine (Adenosine, Life Medical AB, Stockholm) and in subsequent rest. Adenosine response is assessed clinically based on symptoms and heart rate response. Adenosine and contrast agent are administered in two different cannulas. Subjects abstained from caffeine for 24 hours prior to CMR examination. A distributed tissue exchange model is used to compute the perfusion maps and the Gadgetron (reconstruction computer) inline perfusion mapping software is used to generate the perfusion maps.Typical imaging parameters were bSSFP single shot readout, flip angel 50°, slice thickness 8.0 mm, TE/TR 1.04/2.5 ms, bandwidth 1085 Hz/pixel, FOV 360 × 270 mm2 and saturation delay/trigger delay (TD) 95/40 ms.

Officiële titel

Att Överleva Och Leva Som Vuxen Med Enkammarhjärta I Sverige

Aandoeningen
Univentriculair hartMicrovasculaire disfunctieHartfalenMagnetic Resonance
Publicaties
Wetenschappelijke artikelen en onderzoekspapers gepubliceerd over deze klinische studie:
Andere studie-ID's
  • CMR_TCPC
  • Dnr 2022-04574-01
NCT-ID
Startdatum (Werkelijk)
2024-04-15
Laatste update geplaatst
2024-12-16
Verwachte einddatum
2025-09-01
Inschrijving (Geschat)
30
Studietype
Observationeel
Status
Recruterend
Trefwoorden
Fontan circulation
CMR
stress-perfusion
tissue characterization
univentricle heart
TCPC
Armen / Interventies
Deelnemersgroep/StudiearmInterventie/Behandeling
Univentricle heart, operated with TCPC (total cavo pulmonary connection)
Cardiac Magnetic Resonance Stress-perfusion
Included patients will be examined at the Karolinska University Hospital in a 1.5T Siemens Sola magnetic resonance camera at rest and during adenosine stress with specific CMR sequences (adenosine stress-perfusion, myocardial velocities, and tissue characterization) for non-invasive determination of macro- and microvascular dysfunction, global myocardial function, pulmonary artery pressure and scarring of the myocardium. Adenosine or Regadenoson will be used as stress medication which is according to clinical routine. Adenosine will be infused over approximately 5 minutes (110-140 μg / kg/min), Regadenoson (5 ml) will be a 10-second injection (400 μg single dosage). Intravenous gadolinium-based contrast agents will be administered, Gadovist (1 mmol/ml, gadobuterol), 0.15 mmol/kg during stress and rest.
Primaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
Detection of microvascular dysfunction in patients with UVH
This project aims to evaluate microvascular dysfunction using quantitative stress-perfusion CMR in patients with different morphological systemic chamber (left vs right).
Through study completion, an average of 1 year
Secundaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
To detect and compare tissue characterization.
Investigate whether positive findings in tissue characterization is higher in different systemic ventricles (left vs right) using T1 and T2-mapping, LGE (late gadolinium enhancement, myocardial scar).
Through study completion, an average of 1 year
Geschiktheidscriteria

Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
18 Years
Geslachten die in aanmerking komen voor de studie
Allen
  • Patients who had undergone total cavo-pulmonary connection (TCPC) surgery resulting in Fontan circulation.
  • NYHA (New York Heart Assosiation) class I-II.
  • Understanding the study information (signed informed consent).
  • >18 years old.

  • Device therapy (pacemaker, ICD).
  • Failing Fontan (NYHA III-IV).
  • Kidney failure (GFR<30ml/h).
  • Arrythmia (atrial fibrillation).
  • Pregnancy.
Karolinska Institutet logoKarolinska Instituut
Karolinska University Hospital logoKarolinska University Hospital
Verantwoordelijke instantie
Peder Sörensson, Hoofdonderzoeker, Senior Consultant in Cardiology, Karolinska Institutet
Centraal Contactpersoon
Contact: Peder Sorensson, MD, Associate professor, +46 731 400059, [email protected]
Contact: Ayse-Gul Ozturk, MD, [email protected]
1 Studielocaties in 1 landen
Karolinska University Hospital, Stockholm, 17176, Sweden
Peder Sorensson, MD, Associate professor, Contact, +46 731 400059, [email protected]
Ayse-Gul Ozturk, MD, Contact, +46 72 578 02 72, [email protected]
Peder Sorensson, MD, Associate professor, Contact
Recruterend