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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:
- 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
- 负责人:
- 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
- 负责人:
- 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
- 负责人:
- 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:
- 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:
- 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
- 负责人:
- 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
- 负责人:
- 关键词:
- 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
- 负责人:
- 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:
- 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