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急性冠症候群の症状を有する参加者を対象としたElecsys® Troponin T hs Gen 6の研究
基本情報
- NCT ID
- NCT06734117
- ステータス
- 完了
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 5,429
- 治験依頼者名
- Hoffmann-La Roche
概要
This prospective, non-interventional, single arm, longitudinal cohort multicenter study will recruit approximately 5600 consecutive all-comers, consisting of patients with signs and symptoms of acute coronary syndromes (ACS) who present in the emergency department (ED). The main objective of the study is to determine the clinical performance of Elecsys Troponin T hs Gen 6 versus the centrally adjudicated clinical diagnosis at various time points after ED presentation using the previously determined clinical cut-off of a universal 99th percentile upper reference limit.
対象疾患
Acute Coronary SyndromeMyocardial Infarction
介入
Elecsys® Troponin T hs Gen 6(DIAGNOSTIC_TEST)
Blood sample collection(PROCEDURE)
依頼者(Sponsor)
実施施設 (3)
近江八幡市立総合医療センター
Ōmihachiman, Japan
東京ベイ・浦安市川医療センター
Chiba, Japan
公益財団法人大原記念倉敷中央医療機構 倉敷中央病院
Okayama, Japan