Artículo de publicación ISIObjectives We conducted a systematic survey of the methodological literature to identify recommended approaches for how and what randomised clinical trial (RCT) authors should report on missing participant data and, on the basis of these approaches, to propose guidance for RCT authors. Methods We defined missing participant data (MPD) as missing outcome data for trial participants. We considered both categorical and continuous outcome data. We searched MEDLINE and the Cochrane Methodology Register for articles in which authors proposed approaches to reporting MPD from RCTs. We selected eligible articles independently and in duplicate and extracted data in duplicate. Using an iterative process of discussion and...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
Objectives To analyse the amount, reporting and handling of missing data, approach to intention-to-t...
The clinical study with no missing data has yet to be conducted – and never will be! Yet, despite it...
Artículo de publicación ISIObjectives We conducted a systematic survey of the methodological literat...
BACKGROUND AND OBJECTIVES: In order for authors of systematic reviews to address missing data in ran...
Objective: To assess analytic approaches randomized controlled trial (RCT) authors use to address mi...
Abstract Background When potentially associated with ...
Missing data is a potential source of bias in the results of randomised controlled trials (RCTs), wh...
Evidence-based research in health care has been developed well in recent years. One of the biggest c...
Missing outcome data of trial participants is a frequent phenomenon in RCTs and may represent a seri...
UA Open Access Publishing FundBackground Missing outcome data is a threat to the validity of treatme...
<div><p>Background</p><p>Study publication bias and outcome reporting bias have been recognised as t...
UA Open Access Publishing Fund.Introduction: Cluster randomised trials (CRTs) randomise participants...
Artículo de publicación ISIObjectives: To describe how systematic reviewers are reporting missing da...
Objectives Missing data represent a source of bias in randomized clinical trials (RCTs). This thesi...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
Objectives To analyse the amount, reporting and handling of missing data, approach to intention-to-t...
The clinical study with no missing data has yet to be conducted – and never will be! Yet, despite it...
Artículo de publicación ISIObjectives We conducted a systematic survey of the methodological literat...
BACKGROUND AND OBJECTIVES: In order for authors of systematic reviews to address missing data in ran...
Objective: To assess analytic approaches randomized controlled trial (RCT) authors use to address mi...
Abstract Background When potentially associated with ...
Missing data is a potential source of bias in the results of randomised controlled trials (RCTs), wh...
Evidence-based research in health care has been developed well in recent years. One of the biggest c...
Missing outcome data of trial participants is a frequent phenomenon in RCTs and may represent a seri...
UA Open Access Publishing FundBackground Missing outcome data is a threat to the validity of treatme...
<div><p>Background</p><p>Study publication bias and outcome reporting bias have been recognised as t...
UA Open Access Publishing Fund.Introduction: Cluster randomised trials (CRTs) randomise participants...
Artículo de publicación ISIObjectives: To describe how systematic reviewers are reporting missing da...
Objectives Missing data represent a source of bias in randomized clinical trials (RCTs). This thesi...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
Objectives To analyse the amount, reporting and handling of missing data, approach to intention-to-t...
The clinical study with no missing data has yet to be conducted – and never will be! Yet, despite it...