Observational Study of the Remodelling Process Following Myocardial Infarct
Assessment of the Relationship Between Collagen Turnover, Left Ventricular Remodelling and Myocardial Scarring Assessed by Cardiac Magnetic Resonance and Neurohumoral Activation in Patients With Previous Myocardial Infarction
調査の概要
詳細な説明
A multinational trial compared losartan vs. captopril in 5477 postinfarction patients with symptoms of heart failure and/or evidence of left ventricular dysfunction. The trial was terminated in 2002 and the results of the main trial have been published. In this trial, a collagen and neurohumoral substudy was performed to assess the importance of collagen turnover in this population. A total of 235 patients were included from 18 centres. Blood was taken at randomisation, 1 month, 1 year and 2 years.
The present study will recruit surviving patients among the 119 individuals that were randomised to the neurohumoral substudy at the Stavanger University Hospital. The study will assess the relationship between collagen turnover, neurohormonal activation, scarring and left ventricle remodelling in these patients about 3 years following the index myocardial infarction.
The data collected at the 3-year follow-up visit will be compared to data from the initial study.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Stavanger、ノルウェー、NO-4011
- Stavanger University Hospital
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Participation in the previous neurohormonal substudy of the OPTIMAAL trial
- Willingness to participate in the present study and ability to understand and sign the written informed consent
Exclusion Criteria:
- Myocardial infarction within 3 months of visit 1.
- Significant primary valve disease, confirmed by ECHO cardiography,
- Autoimmune disease likely to cause an increase in collagen turnover
- Active cancer disease
- Immunosuppressive treatment,
- Significantly reduced liver function
- Contraindications for performing a cardiac MRI scan (including claustrophobia, implanted ferromagnetic devices or known allergic reactions to Omniscan™).
- Inability to cooperate during the 1 month follow up period.
研究計画
研究はどのように設計されていますか？
デザインの詳細
協力者と研究者
スポンサー
捜査官
- 主任研究者：Kenneth Dickstein, PhD、Helse Stavanger HF
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- StaHF461302
- Helse Vest 911017 (その他の助成金/資金番号：Helse Vest RHF)
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