Authors |
Contact details for the corresponding author |
Trial design |
Description of the trial design (such as parallel, cluster, non-inferiority) |
Methods: |
|
Participants |
Eligibility criteria for participants and the settings where the data were collected |
Interventions |
Interventions intended for each group |
Objective |
Specific objective or hypothesis |
Outcome |
Clearly defined primary outcome for this report |
Randomisation |
How participants were allocated to interventions |
Blinding (masking) |
Whether participants, care givers, and those assessing the outcomes were blinded to group assignment |
Results: |
|
Numbers randomised |
Number of participants randomised to each group |
Recruitment |
Trial status |
Numbers analysed |
Number of participants analysed in each group |
Outcome |
For the primary outcome, a result for each group and the estimated effect size and its precision |
Harms |
Important adverse events or side effects |
Conclusions |
General interpretation of the results |
Trial registration |
Registration number and name of trial register |
Funding |
Source of funding |