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Data from: Publication and reporting of clinical trial results: cross sectional analysis across academic medical centers
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DOI:
doi:10.5061/dryad.6n018
摘要:
e is poor performance and noticeable variation in the dissemination of clinical trial results across leading academic medical centers.
Data from: A critical appraisal of clinical trials conducted and subsequent drug approvals in India and South Africa
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Ethics (see Medical Ethics);Clinical Trials;Protocols & guidelines;1st January 2005 to 31st December 2010
DOI:
doi:10.5061/dryad.013hq
摘要:
/USA without a New Drug Application (NDA) approval in India or South Africa. Conclusions: Despite an increase in clinical trial activities, ther
Data from: Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials
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关键词:
Consensus;Amyotrophic Lateral Sclerosis;guidelines;modified Delphi process;Clinical Trials
DOI:
doi:10.5061/dryad.32q9q5d
摘要:
; 5. Recruitment and retention; 6. Biomarkers; 7. Clinical trial phases; 8. Beyond traditional trial designs; and 9. Statistical considerations. Assigned to one
Data from: Evaluating adherence to the International Committee of Medical Journal Editors’ policy of mandatory, timely clinical trial registration
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关键词:
trialome;clinical research informatics
DOI:
doi:10.5061/dryad.1q030
摘要:
s and Methods: Observational study using computerized analysis of publicly available MEDLINE article data and clinical trial registry data. We anal
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: 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:
without significantly reducing willingness to participate in hypothetical clinical trials. Methods:?This prospective randomized trial was conducted from 2015
Data from: Sharing of clinical trial data among trialists: a cross sectional survey
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关键词:
Biomedical Research Trials;Data sharing;Clinical Trials
DOI:
doi:10.5061/dryad.6544v
摘要:
Objective: To investigate clinical trialists’ opinions and experiences of sharing of clinical trial data with investigators who are not directly
Data from: Clinical trial registration, reporting, publication and FDAAA compliance: a cross-sectional analysis and ranking of new drugs approved
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DOI:
doi:10.5061/dryad.t8n07
摘要:
Objective: To evaluate clinical trial registration, reporting and publication rates for new drugs by: (1) legal requirements and (2) the ethical
Data from: Risk factors for suicidality in Huntington's disease: an analysis of the 2CARE clinical trial
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关键词:
164 Huntington's disease;Suicidality;Huntington's disease;All Clinical trials; 19 All Clinical trials
DOI:
doi:10.5061/dryad.2hp4hq3
摘要:
e limited. We analyzed 609 participants from 2CARE, a randomized, double-blind, placebo controlled clinical trial with up to 5 years of follow
Data from: Quality expectations and tolerance limits of trial master files (TMF) - Developing a risk-based approach for quality assessments of TMFs
负责人:
关键词:
Quality Risk Management;clinical trial;Trial Master File
DOI:
doi:10.5061/dryad.t2f61
摘要:
s the TMF need to have so that a clinical trial can be adequately reconstructed from documented data and procedures? Clinical trial sponsors face significa

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