Objective: To assess analytic approaches randomized controlled trial (RCT) authors use to address missing participant data (MPD) for patient-important continuous outcomes. Study Design and Setting: We conducted a systematic survey of RCTs published in 2014 in the core clinical journals that reported at least one patient-important outcome analyzed as a continuous variable. Results: Among 200 studies, 187 (93.5%) trials explicitly reported whether MPD occurred. In the 163 (81.5%) trials that reported the occurrence of MPD, the median and interquartile ranges of the percentage of participants with MPD were 11.4% (2.5%-22.6%).Among the 147 trials in which authors made clear their analytical approach to MPD, the approaches chosen include...
OBJECTIVE: To characterise the percentage of available outcome data being presented in reports of ra...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
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...
Missing data is a potential source of bias in the results of randomised controlled trials (RCTs), wh...
Abstract Background When potentially associated with ...
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...
Objectives Missing data represent a source of bias in randomized clinical trials (RCTs). This thesi...
Purpose: Patient reported outcome measures (PROMs) are designed to assess patients' perceived health...
Objectives: To describe how systematic review authors report and address categories of participants ...
Evidence-based research in health care has been developed well in recent years. One of the biggest c...
Background/aims: After completion of a randomised controlled trial, an extended follow-up period may...
OBJECTIVE: To characterise the percentage of available outcome data being presented in reports of ra...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
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...
Missing data is a potential source of bias in the results of randomised controlled trials (RCTs), wh...
Abstract Background When potentially associated with ...
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...
Objectives Missing data represent a source of bias in randomized clinical trials (RCTs). This thesi...
Purpose: Patient reported outcome measures (PROMs) are designed to assess patients' perceived health...
Objectives: To describe how systematic review authors report and address categories of participants ...
Evidence-based research in health care has been developed well in recent years. One of the biggest c...
Background/aims: After completion of a randomised controlled trial, an extended follow-up period may...
OBJECTIVE: To characterise the percentage of available outcome data being presented in reports of ra...
markdownabstractThe clinical study with no missing data has yet to be conducted – and never will be!...
The clinical study with no missing data has yet to be conducted – and never will be! Yet, despite it...