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Red blood cell membrane fatty acids and platelet functions (platelet aggregation and dense granule secretion) were monitored at baseline, 1-, 3- and 6-months.
Through physical therapy sessions, hemodynamic and respiratory parameters, along with pain scores, were monitored at baseline, as well as at 0 and 15 min afterward, respectively.
Plasma HIV-1 RNA measurements (lower limit of quantification 50 copies/mL), CD4 cells, routine hematology and chemistry were monitored at baseline, after 1 and 3 months of treatment, and every three months thereafter.
Arterial blood pressure was monitored at baseline, immediately post reperfusion, one, and 6 weeks post MI.
Cardiac function was monitored at baseline and serially in all patients enrolled in the study.
Serum testosterone levels were monitored at baseline, after 12 weeks, after 24 weeks, and monthly thereafter.
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A model including conscientiousness and age significantly predicted 7% of the variance in blood glucose monitoring at baseline [ R = 0.07; F(2, 118) = 4.10; P = 0.02].
Unlike most previous studies we used the ideal method of ambulatory blood pressure monitoring at baseline and for measuring the primary outcome.
This study included a unique population of children, adolescents, and adults with type 1 diabetes as noted by their entry A1C levels being <7.0% and their attention to intensive diabetes management principles with frequent blood glucose monitoring at baseline, averaging about seven times per day.
A clinical followup including sIgE and blood samples for the measurement of protein levels was collected and monitored at different timelines (baseline and 6 and 12 months) for every patient.
The patients were monitored at this fixed baseline heart rate for 30 min with measurements of ECG, blood pressure, cardiac output, ventilation, ETCO2, and end-tidal O2 (ETO2) recorded to confirm stable baseline respiratory control with no evidence of respiratory oscillations suggestive of periodic breathing.
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