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Table 1 shows the schedule of assessment.
The full schedule of assessment and procedures is shown in the table 1.
This study used dosage of 160 mgs soybean isoflavone for treatment group and 0 mg for placebo group for 12 weeks, and the sample consisted of 40 persons that is randomized into 2 groups i.e. control group and treatment group and in order to restrict drop out then a follow up was performed using schedule of assessment visit guidelines.
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This report outlines procedures for data collection and presents the recommended minimum schedule of assessments that comprise the disease-specific clinical and laboratory parameters that are tracked in the database.
Safety of the injected study materials was determined as the incidence of adverse events and the occurrence of significant clinical, haematological and biochemical abnormalities during the procedure and at the intervals indicated in the schedule of assessments.
Table 1 presents the schedule of assessments and procedures.
The schedule of assessments is provided in Table 3.
The schedule of assessments is described in Figure 2.
The schedule of assessments is presented in Table 1.
The time schedule of assessments of participants is shown in table 1.
Follow-up of the subjects was not limited by the study's schedule of assessments.
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