Condition: ATTR-CM · Sponsor: AstraZeneca
This multicenter, prospective, single-arm, interventional study will enroll about 4,000 adult patients at high risk of ATTR amyloidosis from around 50 sites in China. Eligible patients are aged ≥60 years and have documented symptomatic heart failure with left ventricular ejection fraction ≥40% and LVH. Exclusion criteria include known etiologies of myocardial diseases, anomalies of serum free light chain or serum immunofixation electrophoresis, acute myocardial infarction within 6 months before screening, and inability to undergo 99mTc-PYP. Patients will undergo a 14-week diagnostic process. The study intervention involves knowledge training, operation training and post-training verification among investigators. Knowledge training for CV department investigators will cover disease-specific knowledge, standard diagnostic pathways, and genetics; training for investigators in echocardiology (ECHO) and nuclear medicine departments will focus on disease knowledge, standardized operating procedures (SOPs), and imaging parameter reporting. Operation training includes hands-on training in SOPs and image interpretation for ECHO and nuclear medicine investigators. Post-training verification will assess site-level compliance. Extra training will be arranged if quality audit is off target. The primary endpoint is the proportion of patients diagnosed with ATTR amyloidosis in high-risk populations. Secondary endpoints include the proportion of patients with ATTRwt amyloidosis, concordanc…
This description comes directly from the study's public registry record.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
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| Research Site | Beijing, China | Not Yet Recruiting |
| Research Site | Beijing, China | Not Yet Recruiting |
| Research Site | Beijing, China | Not Yet Recruiting |
| Research Site | Beijing, China | Not Yet Recruiting |
| Research Site | Beijing, China | Not Yet Recruiting |
| Research Site | Changlexi, China | Not Yet Recruiting |
| Research Site | Changsha, China | Not Yet Recruiting |
| Research Site | Changsha, China | Not Yet Recruiting |
| Research Site | Changsha, China | Not Yet Recruiting |
| Research Site | Chengdu, China | Not Yet Recruiting |
| Research Site | Chengdu, China | Not Yet Recruiting |
| Research Site | Chongqing, China | Not Yet Recruiting |
+ 36 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07338942