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Effect of intermittent fasting after ST-elevation myocardial infarction on left ventricular function: study protocol of a pilot randomised controlled trial (INTERFAST-MI).
Dutzmann, Jochen; Knöpp, Kai; Kefalianakis, Zoe; Daniel, Jan-Marcus; Gufler, Hubert; Wohlgemuth, Walter; Kahles, Florian; Sedding, Daniel G.
Afiliação
  • Dutzmann J; Department of Internal Medicine III, University Hospital Halle, Halle, Germany.
  • Knöpp K; Department of Internal Medicine III, University Hospital Halle, Halle, Germany.
  • Kefalianakis Z; Department of Internal Medicine III, University Hospital Halle, Halle, Germany.
  • Daniel JM; Department of Internal Medicine III, University Hospital Halle, Halle, Germany.
  • Gufler H; Department of Radiology, University Hospital Halle, Halle, Germany.
  • Wohlgemuth W; Department of Radiology, University Hospital Halle, Halle, Germany.
  • Kahles F; Department of Internal Medicine I, University Hospital Aachen, Aachen, Germany.
  • Sedding DG; Department of Internal Medicine III, University Hospital Halle, Halle, Germany daniel.sedding@uk-halle.de.
BMJ Open ; 12(4): e050067, 2022 04 07.
Article em En | MEDLINE | ID: mdl-35393305
INTRODUCTION: Preclinical studies consistently show robust disease-modifying effects of intermittent fasting in animal models of cardiovascular disease. However, the impact of intermittent fasting on cardiovascular endpoints after myocardial infarction has not been investigated in a clinical trial so far. METHODS AND ANALYSIS: The INTERmittent FASTing after Myocardial Infarction (INTERFAST-MI) trial is a monocentric prospective randomised controlled non-confirmatory pilot study including 48 patients with ST-segment elevation myocardial infarction. They will be randomised in a 1:1 ratio to either intermittent fasting (daily time-restricted eating; consuming food for not more than 8 hours/day, fasting for at least 16 hours/day) or to a control group without a particular diet. The follow-up time is 6 months. The prespecified primary outcome is change in left ventricular systolic function at 4 weeks from baseline to estimate effect size required to establishing sample size and power calculation for a future full-scale trial. Secondary outcomes include protocol adherence, recruitment, major adverse cardiac events, revascularisation, changes in left ventricular systolic function at 3 and 6 months, patient weight, blood pressure, and serum markers of inflammation and cardiovascular disease. Enrolment began on 1 November 2020 and is expected to conclude in December 2021. ETHICS AND DISSEMINATION: The trial has received ethics approval from the Medical Ethics Committee of the Martin-Luther-University Halle-Wittenberg. Results of the study will be submitted for publication in a peer-reviewed journal and presented at scientific conferences. TRIAL REGISTRATION NUMBER: DRKS00021784.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infarto do Miocárdio com Supradesnível do Segmento ST / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Guideline / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infarto do Miocárdio com Supradesnível do Segmento ST / Infarto do Miocárdio Tipo de estudo: Clinical_trials / Guideline / Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article