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Data from: Publication and reporting of clinical trial results: cross sectional analysis across academic medical centers
负责人:
关键词:
DOI:
doi:10.5061/dryad.6n018
摘要:
Objective: To determine rates of publication and reporting of results within two years for all completed clinical trials registered in ClinicalTrials
Data from: A critical appraisal of clinical trials conducted and subsequent drug approvals in India and South Africa
负责人:
关键词:
Ethics (see Medical Ethics);Clinical Trials;Protocols & guidelines;1st January 2005 to 31st December 2010
DOI:
doi:10.5061/dryad.013hq
摘要:
Objectives: To assess the relation between the number of clinical trials conducted and respective new drug approvals in India and South Africa
Data from: Overview of phase IV clinical trials for postmarket drug safety surveillance: a status report from the ClinicalTrials.gov registry
负责人:
关键词:
Adverse events;Clinical Trials;Health & safety
DOI:
doi:10.5061/dryad.3t6sc
摘要:
s of contemporary phase IV clinical trials and whether these studies are of sufficient quality to advance medical knowledge in pharmacovigilance. We aimed
Data from: Terminated trials in the ClinicalTrials.gov results database: evaluation of availability of primary outcome data and r
负责人:
关键词:
clinical trial;reporting guideline;ClinicalTrials.gov;transparency;results disclosure;trial termination
DOI:
doi:10.5061/dryad.v5403
摘要:
Background: Clinical trials that end prematurely (or “terminate”) raise financial, ethical, and scientific concerns. The extent to which the result
Data from: Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials
负责人:
关键词:
Consensus;Amyotrophic Lateral Sclerosis;guidelines;modified Delphi process;Clinical Trials
DOI:
doi:10.5061/dryad.32q9q5d
摘要:
and clinical trials in amyotrophic lateral sclerosis (ALS). Methods: A consensus committee comprising 140 key members of the international ALS community (ALS
Data from: Evaluating adherence to the International Committee of Medical Journal Editors’ policy of mandatory, timely clinical trial registration
负责人:
关键词:
trialome;clinical research informatics
DOI:
doi:10.5061/dryad.1q030
摘要:
que international mandate that may be providing a powerful incentive for sponsors and investigators to document clinical trials and trial result publica
Data from: Clinical trial registration, reporting, publication and FDAAA compliance: a cross-sectional analysis and ranking of new drugs approved
负责人:
关键词:
DOI:
doi:10.5061/dryad.t8n07
摘要:
l clinical trials submitted to the Food and Drug Administration (FDA) for drugs approved in 2012, sponsored by large biopharmaceutical companies. Data sources: Inf
Data from: Characteristics of randomised trials on diseases in the digestive system registered in ClinicalTrials.gov - a retrospective analysis
负责人:
关键词:
Statistics & research methods;Clinical Trials;Journalism;Medical journalism
DOI:
doi:10.5061/dryad.s38s0g00
摘要:
Objectives: To evaluate the adequacy of reporting of protocols for randomised trials on diseases of the digestive system registered in ClinicalTrials
Data from: Reducing therapeutic misconception: a randomized intervention trial in hypothetical clinical trials
负责人:
关键词:
therapeutic misconception;informed consent;Clinical Trials
DOI:
doi:10.5061/dryad.60v8b
摘要:
Background:?Participants in clinical trials frequently fail to appreciate key differences between research and clinical care. This phenomenon
Data from: Sharing of clinical trial data among trialists: a cross sectional survey
负责人:
关键词:
Biomedical Research Trials;Data sharing;Clinical Trials
DOI:
doi:10.5061/dryad.6544v
摘要:
s of clinical trials published in 2010 or 2011 in one of six general medical journals with the highest impact factor in 2011. Main outcome measures: Support

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