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No data were attributed for missing data and analyzed for intent to treat.
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Primary and secondary endpoints will be analyzed for the intent-to-treat (ITT) population, which consists of all randomized patients who have a baseline and at least one post-baseline assessment.
The treatment outcomes were analyzed for the intent-to-treat sample with the primary outcome being the percent reduction from baseline to endpoint on the HAMD-17 rating scale, using the last observation carried forward (LOCF) method for interpolating final score for those subjects who discontinued before the final endpoint.
The secondary data were gathered from "documentary-based secondary data, that refer to information collected from previous similar researchers which have also included primary data and have already been analyzed for their original intent" (Saunders et al., 2003).
The intent-to-treat population analyzed for efficacy and safety included all randomized patients who received at least one dose of study medication.
The population analyzed for all efficacy and safety endpoints was the modified intent-to-treat population, which comprised all randomized patients who received at least one dose of study treatment.
Each question is then analyzed for discrimination.
Patients were analyzed by "intent to treat" and were followed for a minimum of 2 yr.
Data were analyzed by intent to treat.
Data were analyzed by intent to treat.Seventy-one patients were randomly assigned.
Patients were analyzed by intent of radiation and toxicity graded based on CTCAE 4.0.
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