Background: Clinical trial registries are in widespread use to promote transparency around trials and their results. Objective: To describe characteristics of drug trials listed in ClinicalTrials.gov and examine whether the funding source of these trials is associated with favorable published outcomes. Design: An observational study of safety and efficacy trials for anticholesteremics, antidepressants, antipsychotics, proton-pump inhibitors, and vasodilators conducted between 2000 and 2006. Setting: ClinicalTrials.gov, a Web-based registry of clinical trials launched in 1999. Measurements: Publications resulting from the trials for the 5 drug categories of interest were identified, and data were abstracted on the trial record and publicatio...
Objective: To determine rates of publication and reporting of results within two years for all compl...
Background: Publication bias of clinical trials can lead to increased harms and costs for patients a...
Background: ClinicalTrials.gov requires reporting of result summa-ries for many drug and device tria...
Background: Clinical trial registries are in widespread use to pro-mote transparency around trials a...
Background: Clinical trial registries are in widespread use to pro-mote transparency around trials a...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
OBJECTIVE: To investigate the distribution, design characteristics, and dissemination of clinical tr...
In 2007, the FDA Amendments Act expanded requirements for ClinicalTrials.gov, a public clinical tria...
Background: The US Food and Drug Administration Amendments Act requires results from clinical trial...
<div><p>Objective</p><p>In an effort to understand how results of human clinical trials are made pub...
OBJECTIVE: In an effort to understand how results of human clinical trials are made public, we analy...
BackgroundRegistration of clinical trials has been introduced largely to reduce bias toward statisti...
BackgroundTo limit selective and incomplete publication of the results of clinical trials, registrie...
Objective: To determine rates of publication and reporting of results within two years for all compl...
Background: Publication bias of clinical trials can lead to increased harms and costs for patients a...
Background: ClinicalTrials.gov requires reporting of result summa-ries for many drug and device tria...
Background: Clinical trial registries are in widespread use to pro-mote transparency around trials a...
Background: Clinical trial registries are in widespread use to pro-mote transparency around trials a...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
At the end of the past century there were multiple concerns regarding lack of transparency in the co...
OBJECTIVE: To investigate the distribution, design characteristics, and dissemination of clinical tr...
In 2007, the FDA Amendments Act expanded requirements for ClinicalTrials.gov, a public clinical tria...
Background: The US Food and Drug Administration Amendments Act requires results from clinical trial...
<div><p>Objective</p><p>In an effort to understand how results of human clinical trials are made pub...
OBJECTIVE: In an effort to understand how results of human clinical trials are made public, we analy...
BackgroundRegistration of clinical trials has been introduced largely to reduce bias toward statisti...
BackgroundTo limit selective and incomplete publication of the results of clinical trials, registrie...
Objective: To determine rates of publication and reporting of results within two years for all compl...
Background: Publication bias of clinical trials can lead to increased harms and costs for patients a...
Background: ClinicalTrials.gov requires reporting of result summa-ries for many drug and device tria...