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The person analyzing all data was blinded to the diagnosis.
Pharmacists and psychiatrists were not blinded to the patients' group allocation but the research assistant who collected all data was blinded to group allocation.
All data was blinded with respect of the patients' identity (name, birthday and address), the name of the departments at the general hospital and the names of the physicians.
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All data were blinded for the examiner calculating the respiratory rates.
The person who analyzed the PET data was blinded from the MRI results.
This data was blinded, allowing data analysis while maintaining the patient confidentiality.
However, the researcher assistant collecting data was blinded to participant allocation throughout the study.
The registrar of the questionnaire data was blinded to group allocation.
After enrollment of patients, data was blinded to avoid potential bias.
The investigator (PW) analyzing the data was blinded to the assigned trial fluids.
The measurements were performed in random order, and all clinical data were blinded to prevent biases.
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