Search Results - "Von Elm, Erik"

Strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies by Elm, Erik von, Altman, Douglas G, Egger, Matthias, Pocock, Stuart J, Gøtzsche, Peter C, Vandenbroucke, Jan P

“…Poor reporting of research hampers assessment and makes it less useful. An international group of methodologists, researchers, and journal editors sets out…”
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The strengthening the reporting of observational studies in epidemiology (STROBE) statement : Guidelines for reporting observational studies by VON ELM, Erik, ALTMAN, Douglas G, EGGER, Matthias, POCOCK, Stuart J, GØTZSCHE, Peter C, VANDENBROUCKE, Jan P

“…Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and…”
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The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies by von Elm, Erik, Altman, Douglas G, Egger, Matthias, Pocock, Stuart J, Gøtzsche, Peter C, Vandenbroucke, Jan P

“…Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and…”
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The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies by von Elm, Erik, Dr, Altman, Douglas G, Prof, Egger, Matthias, Prof, Pocock, Stuart J, Prof, Gøtzsche, Peter C, MD, Vandenbroucke, Jan P, Prof

“…Summary Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and…”
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Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration by Vandenbroucke, Jan P, von Elm, Erik, Altman, Douglas G, Gøtzsche, Peter C, Mulrow, Cynthia D, Pocock, Stuart J, Poole, Charles, Schlesselman, James J, Egger, Matthias

“…Much medical research is observational. The reporting of observational studies is often of insufficient quality. Poor reporting hampers the assessment of the…”
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Systematic review of the empirical evidence of study publication bias and outcome reporting bias by Dwan, Kerry, Altman, Douglas G, Arnaiz, Juan A, Bloom, Jill, Chan, An-Wen, Cronin, Eugenia, Decullier, Evelyne, Easterbrook, Philippa J, Von Elm, Erik, Gamble, Carrol, Ghersi, Davina, Ioannidis, John P A, Simes, John, Williamson, Paula R

“…The increased use of meta-analysis in systematic reviews of healthcare interventions has highlighted several types of bias that can arise during the completion…”
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Insufficient recruitment and premature discontinuation of clinical trials in Switzerland: qualitative study with trialists and other stakeholders by Briel, Matthias, Elger, Bernice, von Elm, Erik, Satalkar, Priya

“…Premature discontinuation occurs in about 25% of randomised clinical trials in Switzerland; it mainly affects investigator-initiated trials and is mostly due…”
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Uncertainties about the need for ethics approval in Switzerland: a mixed-methods study by Gloy, Viktoria, McLennan, Stuart, Rinderknecht, Matthias, Ley, Bettina, Meier, Brigitte, Driessen, Susanne, Gervasoni, Pietro, Hirschel, Bernard, Benkert, Pascal, Gilles, Ingrid, Von Elm, Erik, Briel, Matthias

“…BACKGROUND To ensure ethical oversight, researchers wanting to conduct “research” involving human beings are typically required to obtain prior approval from…”
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How Much Participant Outcome Data Is Missing from Sight: Findings from a Cohort of Trials Submitted to a German Research Ethics Committee by Kirkham, Jamie J, Dwan, Kerry M, Blümle, Anette, von Elm, Erik, Williamson, Paula R

“…Study publication bias and outcome reporting bias have been recognised as two threats to the validity of systematic reviews. The purpose of this research was…”
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Funding characteristics of randomised clinical trials supported by the Swiss National Science Foundation: a retrospective cohort study by Amstutz, Alain, Schandelmaier, Stefan, Frei, Roy, Surina, Jakub, Agarwal, Arnav, Alturki, Reem, von Niederhäusern, Belinda, von Elm, Erik, Briel, Matthias, On Behalf Of The MAking Randomized Trials Affordable Marta Group

“…Failure to publish publicly funded research represents a waste of scarce research resources across medical disciplines and countries. In Switzerland, about 40%…”
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The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement by Benchimol, Eric I, Smeeth, Liam, Guttmann, Astrid, Harron, Katie, Moher, David, Petersen, Irene, Sørensen, Henrik T, von Elm, Erik, Langan, Sinéad M

“…Routinely collected health data, obtained for administrative and clinical purposes without specific a priori research goals, are increasingly used for…”
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The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for reporting observational studies by von Elm, Erik, Altman, Douglas G, Egger, Matthias, Pocock, Stuart J, Gøtzsche, Peter C, Vandenbroucke, Jan P

“…Abstract Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and…”
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Learning from failure--rationale and design for a study about discontinuation of randomized trials (DISCO study) by Kasenda, Benjamin, von Elm, Erik B, You, John, Blümle, Anette, Tomonaga, Yuki, Saccilotto, Ramon, Amstutz, Alain, Bengough, Theresa, Meerpohl, Jörg, Stegert, Mihaela, Tikkinen, Kari A O, Neumann, Ignacio, Carrasco-Labra, Alonso, Faulhaber, Markus, Mulla, Sohail, Mertz, Dominik, Akl, Elie A, Bassler, Dirk, Busse, Jason W, Ferreira-González, Ignacio, Lamontagne, Francois, Nordmann, Alain, Rosenthal, Rachel, Schandelmaier, Stefan, Sun, Xin, Vandvik, Per O, Johnston, Bradley C, Walter, Martin A, Burnand, Bernard, Schwenkglenks, Matthias, Bucher, Heiner C, Guyatt, Gordon H, Briel, Matthias

“…Randomized controlled trials (RCTs) may be discontinued because of apparent harm, benefit, or futility. Other RCTs are discontinued early because of…”
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The reporting of studies conducted using observational routinely collected health data statement for pharmacoepidemiology (RECORD-PE) by Langan, Sinéad M, Schmidt, Sigrún AJ, Wing, Kevin, Ehrenstein, Vera, Nicholls, Stuart G, Filion, Kristian B, Klungel, Olaf, Petersen, Irene, Sorensen, Henrik T, Dixon, William G, Guttmann, Astrid, Harron, Katie, Hemkens, Lars G, Moher, David, Schneeweiss, Sebastian, Smeeth, Liam, Sturkenboom, Miriam, von Elm, Erik, Wang, Shirley V, Benchimol, Eric I

“…In pharmacoepidemiology, routinely collected data from electronic health records (including primary care databases, registries, and administrative healthcare…”
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Switzerland voted against a universal basic income by von Elm, Erik

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Systematic review finds that study data not published in full text articles have unclear impact on meta-analyses results in medical research by Schmucker, Christine M, Blümle, Anette, Schell, Lisa K, Schwarzer, Guido, Oeller, Patrick, Cabrera, Laura, von Elm, Erik, Briel, Matthias, Meerpohl, Joerg J

“…A meta-analysis as part of a systematic review aims to provide a thorough, comprehensive and unbiased statistical summary of data from the literature. However,…”
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The REporting of Studies Conducted Using Observational Routinely-Collected Health Data (RECORD) Statement: Methods for Arriving at Consensus and Developing Reporting Guidelines by Nicholls, Stuart G, Quach, Pauline, von Elm, Erik, Guttmann, Astrid, Moher, David, Petersen, Irene, Sørensen, Henrik T, Smeeth, Liam, Langan, Sinéad M, Benchimol, Eric I

“…Routinely collected health data, collected for administrative and clinical purposes, without specific a priori research questions, are increasingly used for…”
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The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies by von Elm, Erik, Altman, Douglas G, Egger, Matthias, Pocock, Stuart J, Gøtzsche, Peter C, Vandenbroucke, Jan P

“…Abstract Much of biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and…”
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Trial results reporting: FDA Amendments Act Final Rule needs enforcement by von Elm, Erik, Meerpohl, Joerg J

“…1 The Final Rule clarified the scope of the FDAAA, and added requirements such as reporting of detailed adverse event information and inclusion of the full…”
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Comparison of randomized controlled trials discontinued or revised for poor recruitment and completed trials with the same research question: a matched qualitative study by Briel, Matthias, Speich, Benjamin, von Elm, Erik, Gloy, Viktoria

“…More than a quarter of randomized controlled trials (RCTs) are prematurely discontinued, mostly due to poor recruitment of patients. In this study, we…”
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