Phase
Condition
Sarcoidosis
Treatment
PET/MRI
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age ≥ 18 years
Sarcoidosis defined according to ATS/ERS/WASOG criteria
Suspicion of cardiac involvement in sarcoidosis:
Clinical manifestations (syncope, lipothymia, persistent palpitations, signs ofheart failure) and/or
Cardiac rhythm or conduction disorder (Mobitz type 2 atrioventricular block (AVB), AVB 3, right or left bundle branch block, Q wave in at least 2 leads,ventricular arrhythmia (ventricular mono/polymorphic complexes> 1000 per 24 h,ventricular tachycardia, ventricular fibrillation), unexplained sustained VT orepsilon wave) and/or
Compatible cardiac ultrasound abnormality: left ventricular dilatation, septalthickening or wall thinning (especially basal), segmental kinetic disorder andwall aneurysm without coronary anomaly, altered left ventricular ejectionfraction, altered diastolic function, altered right ventricular systolicfunction.
Informed patient consent
Membership of a social security scheme
Exclusion
Exclusion Criteria:
Psychiatric illness not controlled by treatment
Claustrophobia
Known pregnancy or breast-feeding patient
Unbalanced diabetes (influence on carbohydrate metabolism for PET)
Previous infarction or known coronary disease
Known allergy to gadolinium and fluoro-desoxyglucose and their excipients
Renal insufficiency (Clairance < 30 mL/min/1.73m2)
Implanted pacemaker not compatible with a 3 Teslas magnetic field
Patients with ocular metallic foreign bodies, pacemakers, neurostimulators, cochlearimplants, metallic heart valves, vascular clips formerly implanted on cranialaneurysms and, in general, any non-removably implanted electronic medical equipment
Inability or refusal to follow a low-carbohydrate diet for 24 hours, followed by a 6-hour fast required prior to the examination
Patient unable to hold a 10-second apnea.
Patient deprived of liberty by judicial or administrative decision
Patient under legal protection (guardianship, curatorship)
Participation in other interventional research involving the human person or beingin the exclusion period following previous research involving the human person
Patients under AME
Exclusion criteria (post signature of consent) for women of reproductive age :
- Positive pregnancy test result after inclusion
Study Design
Connect with a study center
Henri Mondor Hospital
Créteil,
FranceActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.