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Table 1 Checklist of items to include when reporting a randomized trial

From: The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials

PAPER SECTION Item Descriptor Reported
And topic #   on page #
TITLE & ABSTRACT 1 How participants were allocated to interventions (e.g., random allocation", "randomized", or "randomly assigned").  
Background 2 Scientific background and explanation of rationale.  
Participants 3 Eligibility criteria for participants and the settings and locations where the data were collected.  
Interventions 4 Precise details of the interventions intended for each group and how and when they were actually administered.  
Objectives 5 Specific objectives and hypotheses.  
Outcomes 6 Clearly defined primary and secondary outcome measures and, when applicable,  
   any methods used to enhance the quality of measurements (e.g., multiple observations, training of assessors).  
Sample size 7 How sample size was determined and, when applicable, explanation of any interim analyses and stopping rules.  
Sequence generation 8 Method used to generate the random allocation sequence, including details of any restriction (e.g., blocking, stratification).  
Allocation concealment 9 Method used to implement the random allocation sequence (e.g., numbered  
   containers or central telephone), clarifying whether the sequence was concealed until interventions were assigned.  
Implementation 10 Who generated the allocation sequence, who enrolled participants, and who assigned participants to their groups.  
Blinding (Masking) 11 Whether or not participants, those administering the interventions, and those assessing the outcomes were blinded to group assignment. If done, how the success of blinding was evaluated.  
Statistical methods 12 Statistical methods used to compare groups for primary outcome(s); Methods for additional analyses, such as subgroup analyses and adjusted analyses.  
Participant flow 13 Flow of participants through each stage (a diagram is strongly recommended). Specifically, for each group report the numbers of participants randomly assigned, receiving intended treatment, completing the study protocol, and analyzed for the primary outcome. Describe protocol deviations from study as planned, together with reasons.  
Recruitment 14 Dates defining the periods of recruitment and follow-up.  
Baseline data 15 Baseline demographic and clinical characteristics of each group.  
Numbers analyzed 16 Number of participants (denominator) in each group included in each analysis and whether the analysis was by intention-to-treat". State the results in absolute numbers when feasible (e.g., 10/20, not 50%).  
Outcomes and Estimation 17 For each primary and secondary outcome, a summary of results for each group, and the estimated effect size and its precision (e.g., 95% confidence interval).  
Ancillary analyses 18 Address multiplicity by reporting any other analyses performed, including subgroup analyses and adjusted analyses, indicating those pre-specified and those exploratory.  
Adverse events 19 All important adverse events or side effects in each intervention group.  
Interpretation 20 Interpretation of the results, taking into account study hypotheses, sources of potential bias or imprecision and the dangers associated with multiplicity of analyses and outcomes.  
Generalizability 21 Generalizability (external validity) of the trial findings.  
Overall evidence 22 General interpretation of the results in the context of current evidence.