GA participated in laboratory work, collection and interpretation of laboratory data.
The availability of laboratory data varied between studies in terms of parameters measured and time of sample collection.
Safety assessments included recording of AEs and serious adverse events (SAEs) with severity and relationship to study drug; collection of clinical laboratory data for urinalysis, hematology, and blood chemistry (including serum potassium and plasma glucose); and regular assessments of vital signs, ECGs, and body weight.
Upon recruitment, patients were asked to provide blood samples for the collection of laboratory and serological data and provide psychological and clinical information.
AM: conception of the research idea, study design, data collection and analysis and interpretation and the drafting of the manuscript; AK, BM, FM, EI: study design and analysis, interpret the data and reviewed the manuscript; BA, AG, MA, YB, FB, ZH: data collection, part of laboratory work, data analysis and reviewed the manuscript.
The calculation of Stewart's parameters is cumbersome, however, and involves the collection of several nonroutine laboratory data.
X.F., H.B. and R.Z. conceived the experiments and oversaw the collection of field and laboratory data.
BYK and KJK contributed to the collection of clinical and laboratory data.
