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18F-MFBG PET/CT imaging to evaluate cardiac sympathetic activity: a prospective, single-center clinical cohort study

18F-MFBG PET/CT imaging to evaluate cardiac sympathetic activity: a prospective, single-center clinical cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124477
Enrollment
Unknown
Registered
2026-05-13
Start date
2026-05-15
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Patients with impaired cardiac sympathetic activity

Interventions

18F-MFBG PET / CT imaging group:None

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1. The study participants voluntarily or legal guardians agree to participate in this trial and sign an informed consent form; 2. Age >=18 years and <=95 years (the date of signing the informed consent form) is not limited to gender; 3. Meet the diagnostic criteria for cardiovascular diseases such as hypertension, coronary artery disease, heart failure, and arrhythmia, or other patients such as PD and DLB that can cause impaired cardiac sympathetic nerve activity; 4. Expected survival time to exceed 12 months; 5. Willing and able to comply with diagnostic plans, clinical laboratory tests and other trial procedures.

Exclusion criteria

Exclusion criteria: 1. Known to allergies to injections or their auxiliary agents; 2. Can't lie flat or stay still while performing a PET scan, or be intolerant of a PET scan; 3. Study participants had abnormalities in physical examinations, ECG and clinical laboratory examinations during the screening period, which, as determined by the investigator, may affect safety or compliance; 4. The researchers believe that it is not suitable to participate in this experiment;

Design outcomes

Primary

MeasureTime frame
The ratio of heart to mediastinum (H/M);sensitivity;

Secondary

MeasureTime frame
Elution rate (WR);

Countries

China

Contacts

Public ContactYang Hongjie

Peking University Shenzhen Hospital

yanghongjie7891@163.com+86 15994817126

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026