Completeness of reporting of patient-relevant clinical trial outcomes: comparison of unpublished clinical study reports with publicly available data - Wikidata - thesis-toulmin - TriplyDB

Completeness of reporting of patient-relevant clinical trial outcomes: comparison of unpublished clinical study reports with publicly available data

Completeness of reporting of patient-relevant clinical trial outcomes: comparison of unpublished clinical study reports with publicly available data

http://www.wikidata.org/entity/Q28534273

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Suicidality and aggression during antidepressant treatment: systematic review and meta-analyses based on clinical study reports Challenges and Opportunities for Exploring Patient-Level Data Statins for primary cardiovascular prevention in the elderly OpenTrials: towards a collaborative open database of all available information on all clinical trials Published and unpublished evidence in coverage decision-making for pharmaceuticals in Europe: existing approaches and way forward.Quality and quantity of information in summary basis of decision documents issued by health Canada Assessment of Adverse Events in Protocols, Clinical Study Reports, and Published Papers of Trials of Orlistat: A Document Analysis Reporting of Adverse Events in Published and Unpublished Studies of Health Care Interventions: A Systematic Review Clinical research data sharing: what an open science world means for researchers involved in evidence synthesis Increasing value and reducing waste: addressing inaccessible research Moving forward from rhBMP-2: open science and data sharing Information on new drugs at market entry: retrospective analysis of health technology assessment reports versus regulatory reports, journal publications, and registry reports.Differences in reporting serious adverse events in industry sponsored clinical trial registries and journal articles on antidepressant and antipsychotic drugs: a cross-sectional study How to get all trials reported: audit, better data, and individual accountability.Benefits and harms in clinical trials of duloxetine for treatment of major depressive disorder: comparison of clinical study reports, trial registries, and publications.Risk of bias in industry-funded oseltamivir trials: comparison of core reports versus full clinical study reports Impact of inclusion of industry trial results registries as an information source for systematic reviews.Outcomes in Cochrane systematic reviews addressing four common eye conditions: an evaluation of completeness and comparability.Understanding adverse drug reactions in package leaflets - an exploratory survey among health care professionals.Antidepressant use and risk of epilepsy and seizures in people aged 20 to 64 years: cohort study using a primary care database.Against vaccine assay secrecy.Publication and non-publication of drug trial results: a 10-year cohort of trials in Norwegian general practice.Consolidated Standards of Reporting Trials (CONSORT): considerations for neuropsychological research.Celebrating 20 years of evidence from the Cochrane Collaboration: what has been the impact of systematic reviews on nephrology?Clinical trial transparency: many gains but access to evidence for new medicines remains imperfect.QUALITY OF SAMPLE SIZE ESTIMATION IN TRIALS OF MEDICAL DEVICES: HIGH-RISK DEVICES FOR NEUROLOGICAL CONDITIONS AS EXAMPLE.Reporting of harms outcomes: a comparison of journal publications with unpublished clinical study reports of orlistat trials Commentary on Berlin et al.Identifying problematic drugs based on the characteristics of their targets Why clinical trial outcomes fail to translate into benefits for patients.An analysis of redactions in Canada's Common Drug Review Clinical Review Reports and how they relate to the patients' voice.Does access to clinical study reports from the European Medicines Agency reduce reporting biases? A systematic review and meta-analysis of randomized controlled trials on the effect of erythropoiesis-stimulating agents in cancer patients.[Benefit assessment of drugs].The use of clinical study reports to enhance the quality of systematic reviews: a survey of systematic review authors Factors associated with clinical trials that fail and opportunities for improving the likelihood of success: A review

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P2860

Completeness of reporting of patient-relevant clinical trial outcomes: comparison of unpublished clinical study reports with publicly available data

http://www.wikidata.org/entity/Q28534273

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2013 nî lūn-bûn

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2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի հոտեմբերին հրատարակված գիտական հոդված

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Michaela F Kerekes

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P2860

Open clinical trial data for all? A view from regulators

Reporting bias in medical research - a narrative review

The imperative to share clinical study reports: recommendations from the Tamiflu experience

Reboxetine for acute treatment of major depression: systematic review and meta-analysis of published and unpublished placebo and selective serotonin reuptake inhibitor controlled trials

Outcome reporting in industry-sponsored trials of gabapentin for off-label use

Dissemination and publication of research findings: an updated review of related biases

Differences in reporting of analyses in internal company documents versus published trial reports: comparisons in industry-sponsored trials in off-label uses of gabapentin

Completeness and changes in registered data and reporting bias of randomized controlled trials in ICMJE journals after trial registration policy

CONSORT 2010 statement: updated guidelines for reporting parallel group randomized trials

Comparison of registered and published primary outcomes in randomized controlled trials.

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