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Study on the content, stability and peak pattern distribution of TTR tetramer in serum of ATTR-CA high risk population

Study on the content, stability and peak pattern distribution of TTR tetramer in serum of ATTR-CA high risk population

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090975
Enrollment
Unknown
Registered
2024-10-16
Start date
2024-10-20
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Transthyroxin protein amyloid cardiomyopathy

Interventions

TTR Normal group:None

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 =90 years old; 2. ATTR-CA high-risk patients, as defined in the 2021 European Society of Cardiology (ESC) Position Statement on the Diagnosis and Treatment of cardiac amyloidosis and the 2023 American College of Cardiology (ACC) Expert Consensus on cardiac amyloidosis, Patients whose left ventricular wall thickness indicated by echocardiography was =12mm and met =1 warning sign of ATTR-CA were defined as ATTR-CA high-risk patients. 3. Sign informed consent, voluntarily participate in the experiment, and agree to participate in visits, examinations, and treatments according to the requirements of the research protocol

Exclusion criteria

Exclusion criteria: 1. Subjects in the tumor active stage, severe infection, acute inflammation, renal failure, severe liver function impairment, and patients who have experienced acute coronary syndrome, unstable angina pectoris, stroke, transient ischemic attack, coronary revasulation, cardiac device implantation, heart valve repair, or major surgery due to worsening heart failure within 1 month; 2. Subjects who have previously received liver and/or heart transplants; (3) Women who are pregnant or breastfeeding; 4. A combination of acute or chronic medical or psychiatric conditions, including recent (within the past year) combination of active suicidal ideation or behavior or abnormalities in laboratory tests, that may increase the risk of adverse events for study participants or interfere with study findings, and are judged by the investigator to be unsuitable for inclusion in the study; 5. Abnormal serum free light chain ratio (?/? 1.65); 6. Abnormal monoclonal immunoglobulin was found by immunofixation electrophoresis of serum protein; 7. Consider other subjects with secondary amyloidosis

Design outcomes

Primary

MeasureTime frame
Cardiovascular death;Cardiovascular rehospitalization;

Countries

China

Contacts

Public ContactYing Liu

The First Affiliated Hospital of Dalian Medical University

www.18098875801@163.com+86 180 9887 5801

Outcome results

None listed

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