Flaws in the design of randomized trials may bias intervention effect estimates and increase between-trial heterogeneity. Empirical evidence suggests that these problems are greatest for subjectively assessed outcomes. For the Risk of Bias in Evidence Synthesis (ROBES) Study, we extracted risk-of-bias judgements (for sequence generation, allocation concealment, blinding, and incomplete data) from a large collection of meta-analyses published in the Cochrane Library (issue 4; April 2011). We categorized outcome measures as mortality, other objective outcome, or subjective outcome, and we estimated associations of bias judgements with intervention effect estimates using Bayesian hierarchical models. Among 2,443 randomized trials in 228 meta-a...
Published evidence suggests that aspects of trial design lead to biased intervention effect estimate...
[EN] Objectives: The aim of this study was to assess the agreement and compare the performance of th...
Risk of bias (ROB) may threaten the internal validity of a clinical trial by distorting the magnitud...
Flaws in the design of randomized trials may bias intervention effect estimates and increase between...
To synthesise evidence on the average bias and heterogeneity associated with reported methodological...
BACKGROUND: The design of randomised controlled trials (RCTs) should incorporate characteristics (su...
Objective: To synthesise evidence on the average bias and heterogeneity associated with reported met...
OBJECTIVE: To examine whether the association of inadequate or unclear allocation concealment and la...
OBJECTIVE: To examine whether the association of inadequate or unclear allocation concealment and la...
Objectives Assess the frequency and reasons for disagreements in risk of bias assessments for random...
International audienceOBJECTIVES: Assess the frequency and reasons for disagreements in risk of bias...
Introduction Meta-epidemiological analyses have demonstrated that reported trial design characterist...
Published evidence suggests that aspects of trial design lead to biased intervention effect estimate...
Background: Systematic reviews of randomised trials guide policy and healthcare decisions. Yet, we o...
Abstract Background Clinical decisions are made based on Cochrane reviews, but the implementation of...
Published evidence suggests that aspects of trial design lead to biased intervention effect estimate...
[EN] Objectives: The aim of this study was to assess the agreement and compare the performance of th...
Risk of bias (ROB) may threaten the internal validity of a clinical trial by distorting the magnitud...
Flaws in the design of randomized trials may bias intervention effect estimates and increase between...
To synthesise evidence on the average bias and heterogeneity associated with reported methodological...
BACKGROUND: The design of randomised controlled trials (RCTs) should incorporate characteristics (su...
Objective: To synthesise evidence on the average bias and heterogeneity associated with reported met...
OBJECTIVE: To examine whether the association of inadequate or unclear allocation concealment and la...
OBJECTIVE: To examine whether the association of inadequate or unclear allocation concealment and la...
Objectives Assess the frequency and reasons for disagreements in risk of bias assessments for random...
International audienceOBJECTIVES: Assess the frequency and reasons for disagreements in risk of bias...
Introduction Meta-epidemiological analyses have demonstrated that reported trial design characterist...
Published evidence suggests that aspects of trial design lead to biased intervention effect estimate...
Background: Systematic reviews of randomised trials guide policy and healthcare decisions. Yet, we o...
Abstract Background Clinical decisions are made based on Cochrane reviews, but the implementation of...
Published evidence suggests that aspects of trial design lead to biased intervention effect estimate...
[EN] Objectives: The aim of this study was to assess the agreement and compare the performance of th...
Risk of bias (ROB) may threaten the internal validity of a clinical trial by distorting the magnitud...