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PETMR myocardial metabolic imaging to assess changes in myocardial glucose metabolism after intensive standard therapy for idiopathic non-ischemic cardiomyopathy

18F-FDG PET/MR myocardial metabolic imaging to assess changes in myocardial glucose metabolism after intensive standard therapy for idiopathic non-ischemic cardiomyopathy

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065511
Enrollment
Unknown
Registered
2022-11-07
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Non-ischemic cardiomyopathy

Interventions

case series:None

Sponsors

The First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. 18 years of age 55 mm (men) or >50 mm (women) (UCG assessment) 3. hypertrophic cardiomyopathy: ventricular wall thickness >= 15 mm in any segment or segments of the left ventricular myocardium and exclusion of other diseases causing increased cardiac load; or previous ventricular wall thickness >= 15 mm in any segment or segments of the myocardium and ventricular wall thickness >= 13 mm in any segment or segments of the myocardium at the time of enrollment; LVEF 1 year 5. participants voluntarily participate in the study and have signed an informed consent form

Exclusion criteria

Exclusion criteria: Candidate participants will be excluded from this study if any of the following conditions are met: 1. diabetes mellitus (fasting serum glucose >= 7.0 mmol/L or glycated hemoglobin >= 6.5%) 2. Stenosis >= 50% on coronary arteriography 3. restrictive cardiomyopathy 4. acute myocarditis, uncontrolled tachyarrhythmia atrial fibrillation, and NYHA class IV The following are not recommended Magnetic resonance imaging is not indicated for metallic objects implanted in the body 5. Severe renal insufficiency (estimated glomerular filtration rate 40g/d for women, >80g/d for men, >5 years of alcohol consumption) 7. Pregnant women, those who are breastfeeding or preparing to conceive 8. Patients who do not want to sign the informed consent form 9. Patients who cannot insist on completing the follow-up visit

Design outcomes

Primary

MeasureTime frame
Compared enrollment, change in FDG uptake values at 3 months after receiving intensive standard drug therapy based on altered cardiac structure compared to enrollment;

Secondary

MeasureTime frame
change in left ventricular function parameters measured by PET/MR at 3-month follow-up;change in right ventricular function parameters measured by PET/MR at 3-month follow-up;Change in estimated pulmonary artery systolic pressure (PASP) measured by UCG at the 3-month follow-up;Changes in heart rate, the width of QRS waves, and QTc interval measured by ECG at the 3-month follow-up visit;Changes in N-terminal B-type natriuretic peptide (NT-proBNP), high-sensitivity troponin (cTnT), and soluble growth-stimulated expression gene 2 protein (soluble ST2) at the 3-month follow-up;Change in 6-minute walk distance (6MWD) measured by 6-minute walk test (6MWT) at the 3-month follow-up;

Countries

China

Contacts

Public ContactWei Sun

The First Affiliated Hospital of Nanjing Medical University

weisun7919@njmu.edu.cn+86 13815860536

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026