[HTML][HTML] The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials
… David Moher, Ken Schulz, and Doug Altman participated in regular conference calls, identified
participants, participated in the CONSORT meetings, and drafted the paper. David Moher …
participants, participated in the CONSORT meetings, and drafted the paper. David Moher …
CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials
Overwhelming evidence shows the quality of reporting of randomised controlled trials (RCTs)
is not optimal. Without transparent reporting, readers cannot judge the reliability and …
is not optimal. Without transparent reporting, readers cannot judge the reliability and …
The revised CONSORT statement for reporting randomized trials: explanation and elaboration
… Even then, however, lack of blinding in any trial can lead to other problems, such as attrition
(Schulz KF, Chalmers I, Altman DG. The landscape and lexicon of blinding. Submitted for …
(Schulz KF, Chalmers I, Altman DG. The landscape and lexicon of blinding. Submitted for …
[HTML][HTML] NASH limits anti-tumour surveillance in immunotherapy-treated HCC
…, F Finkelmeier, O Waidmann, J Trojan, K Schulze… - Nature, 2021 - nature.com
Hepatocellular carcinoma (HCC) can have viral or non-viral causes 1 , 2 , 3 , 4 – 5 . Non-alcoholic
steatohepatitis (NASH) is an important driver of HCC. Immunotherapy has been …
steatohepatitis (NASH) is an important driver of HCC. Immunotherapy has been …
Empirical evidence of bias: dimensions of methodological quality associated with estimates of treatment effects in controlled trials
KF Schulz, I Chalmers, RJ Hayes, DG Altman - Jama, 1995 - jamanetwork.com
Objective. —To determine if inadequate approaches to randomized controlled trial design
and execution are associated with evidence of bias in estimating treatment effects. Design. —…
and execution are associated with evidence of bias in estimating treatment effects. Design. —…
SPIRIT 2013 statement: defining standard protocol items for clinical trials
…, WSM Summerskill, T Groves, KF Schulz… - Annals of internal …, 2013 - acpjournals.org
The protocol of a clinical trial serves as the foundation for study planning, conduct, reporting,
and appraisal. However, trial protocols and existing protocol guidelines vary greatly in …
and appraisal. However, trial protocols and existing protocol guidelines vary greatly in …
SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials
High quality protocols facilitate proper conduct, reporting, and external review of clinical
trials. However, the completeness of trial protocols is often inadequate. To help improve the …
trials. However, the completeness of trial protocols is often inadequate. To help improve the …
CONSORT 2010 statement: updated guidelines for reporting parallel group randomized trials
… Schulz and colleagues describe the latest version, CONSORT 2010, which updates the
reporting guideline based on new methodological evidence and accumulating experience. …
reporting guideline based on new methodological evidence and accumulating experience. …
CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials
Randomised controlled trials, when appropriately designed, conducted and reported,
represent the gold standard in evaluating healthcare interventions. However, randomised trials …
represent the gold standard in evaluating healthcare interventions. However, randomised trials …
Improving the quality of reporting of randomized controlled trials: the CONSORT statement
…, D Moher, I Olkin, R Pitkin, D Rennie, KF Schulz… - Jama, 1996 - jamanetwork.com
… Schulz and colleagues17have shown em¬ pirically that trials in which the alloca¬ tion sequence
had been inadequately … Schulz KF. Subverting randomization in controlled trials. JAMA. …
had been inadequately … Schulz KF. Subverting randomization in controlled trials. JAMA. …