M. Briel

Discipline

Psychologie (4)

Type de document

Articles (20) Recensions (1)

Co-auteur

Date

Source

Mot-clé

recherche (19) Research (19) Research (19) procès (12) Trials (12) information (11) cohorte (11) Human beings (9) Evaluation (9) Publications (9) littérature (8) Reporting (8) Will (8) Literature (8) Design (8) Will (8) Design (8) protocole (7) analyse (7) Research--Moral and ethical aspects (7) Clinical trials (7) Tax assessment (7) Analysis (7) Committees (6) Swiss (6) Patients (6) Medical care (6) Discrimination (6) Committees (6) Size (6)

Documents écrit par M. Briel (20) | parle de M. Briel (0)

Developing and testing a Corona VaccinE tRiAL pLatform (COVERALL) to study Covid-19 vaccine response in immunocompromised patients.
K. Kusejko et al. (28 juil. 2022)
A trial platform to assess approved SARS-CoV-2 vaccines in immunocompromised patients: first sub-protocol for a pilot trial comparing the mRNA vaccines Comirnaty® and COVID-19 mRNA Vaccine Moderna®.
B. Speich et al. (21 oct. 2021)
Comparison of randomized controlled trials discontinued or revised for poor recruitment and completed trials with the same research question: a matched qualitative study.
M. Briel et al. (30 déc. 2019)
Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation.
B. Speich et al. (2019)
Funding characteristics of randomised clinical trials supported by the Swiss National Science Foundation: a retrospective cohort study.
A. Amstutz et al. (2018)
Insufficient recruitment and premature discontinuation of clinical trials in Switzerland: qualitative study with trialists and other stakeholders.
M. Briel et al. (29 nov. 2017)
Discontinuation and non-publication of randomised clinical trials supported by the main public funding body in Switzerland: a retrospective cohort study.
A. Amstutz et al. (1 août 2017)
Systematic review finds that study data not published in full text articles have unclear impact on meta-analyses results in medical research.
C.M. Schmucker et al. (2017)
The reporting of studies using routinely collected health data was often insufficient.
L.G. Hemkens et al.
Bias in dissemination of clinical research findings: structured OPEN framework of what, who and why, based on literature review and expert consensus.
D. Bassler et al. (2016)
Premature Discontinuation of Prospective Clinical Studies Approved by a Research Ethics Committee - A Comparison of Randomised and Non-Randomised Studies.
A. Blümle et al. (2016)
Agreements between Industry and Academia on Publication Rights: A Retrospective Study of Protocols and Publications of Randomized Clinical Trials.
B. Kasenda et al. (2016)
Planning and reporting of quality-of-life outcomes in cancer trials.
S. Schandelmaier et al. (2015)
Subgroup analyses in randomised controlled trials: cohort study on trial protocols and journal publications
B. Kasenda et al. (2014)
Prevalence, characteristics, and publication of discontinued randomized trials.
B. Kasenda et al. (2014)
Defining publication bias: protocol for a systematic review of highly cited articles and proposal for a new framework.
K.F. Müller et al. (2013)
Publication bias in animal research: a systematic review protocol.
M. Briel et al. (2013)
A protocol for a systematic review on the impact of unpublished studies and studies published in the gray literature in meta-analyses.
C. Schmucker et al. (2013)
Detecting, quantifying and adjusting for publication bias in meta-analyses: protocol of a systematic review on methods.
K.F. Mueller et al. (2013)
Learning from failure - rationale and design for a study about discontinuation of randomized trials (DISCO study).
B. Kasenda et al. (2012)