When researchers embark on a clinical trial, they make a commitment to con-duct the trial and to report the findings in accordance with basic ethical prin-ciples. This includes preserving the ac-curacy of the results and making both positive and negative results publicly available.1 However, a significant pro-portion of health-care research remains unpublished and, even when it is pub-lished, some researchers do not make all of their results available.2 Selective reporting, regardless of the reason for it, leads to an incomplete and potentially biased view of a trial and its results.
180), C. B. Fisher equates negative trial results with poorly conducted trials. There is no evi-denc...
Scandals of selective reporting of clinical trial results by pharmaceutical \u85rms have under-lined...
It is both an ethical and a legal requirement that patients who participate in clinical trials must ...
Reports of randomized controlled trials (RCTs) inform the care of future patients and are especially...
Objective: To present a structured account of ethical problems and possible solutions related to sel...
According to the Declaration of Helsinki, as well as the Statement on Public Disclosure of Clinical ...
Objectives: The aim of this study is to review the issues of publication of clinical trials with con...
Theprinciple of data sharingdates to the dawnof sci-entificdiscovery—it ishowresearchers fromdiffere...
Clinical research should ultimately improve patient care. For this to be possible, trials must evalu...
HIGH-PROFILE DISCLOSURES OF“hidden ” data from clinicaltrials have led the public torealize what som...
What would you do if your experiment produced a negative or nonsignificant result? Having a negative...
BACKGROUND: Randomised controlled trials (RCTs) represent the gold standard methodological design to...
BACKGROUND:Research ethicists have recently declared a new ethical imperative: that researchers shou...
Many research-funding agencies now require open access to the results of research they have funded, ...
<div><p>Background</p><p>Access to unpublished clinical study reports (CSRs) is currently being disc...
180), C. B. Fisher equates negative trial results with poorly conducted trials. There is no evi-denc...
Scandals of selective reporting of clinical trial results by pharmaceutical \u85rms have under-lined...
It is both an ethical and a legal requirement that patients who participate in clinical trials must ...
Reports of randomized controlled trials (RCTs) inform the care of future patients and are especially...
Objective: To present a structured account of ethical problems and possible solutions related to sel...
According to the Declaration of Helsinki, as well as the Statement on Public Disclosure of Clinical ...
Objectives: The aim of this study is to review the issues of publication of clinical trials with con...
Theprinciple of data sharingdates to the dawnof sci-entificdiscovery—it ishowresearchers fromdiffere...
Clinical research should ultimately improve patient care. For this to be possible, trials must evalu...
HIGH-PROFILE DISCLOSURES OF“hidden ” data from clinicaltrials have led the public torealize what som...
What would you do if your experiment produced a negative or nonsignificant result? Having a negative...
BACKGROUND: Randomised controlled trials (RCTs) represent the gold standard methodological design to...
BACKGROUND:Research ethicists have recently declared a new ethical imperative: that researchers shou...
Many research-funding agencies now require open access to the results of research they have funded, ...
<div><p>Background</p><p>Access to unpublished clinical study reports (CSRs) is currently being disc...
180), C. B. Fisher equates negative trial results with poorly conducted trials. There is no evi-denc...
Scandals of selective reporting of clinical trial results by pharmaceutical \u85rms have under-lined...
It is both an ethical and a legal requirement that patients who participate in clinical trials must ...