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To avoid sampling other than end-expiratory air, samples were timed to the end-expiratory phase by observation of the patients and the time-flow curve on the ventilation monitor.
Patients were clinically reassessed with scans and laboratory analyses at the end of the observation phase.
At the end of the observation phase, these values had decreased to 173.2, 178.8, and 182.8 mg/dL, respectively.
This ends Phase 1.
Ionospheric delay is excluded by combination of dual-frequency carrier phase observations.
End phase 1 realtime.
Observation periods took place at 7.00 am, 10.00 am, 1.00 pm, 5.00 pm, and 8.00 pm, resulting in two dark-phase observations and three light-phase observations.
The further analyses were strictly performed according to the defined phases by the observed nadirs of mortality rate (phase I: Day 1 until Day 5, phase II: Day 6 until Day 15, phase III: Day 16 until the end of the observation period at Day 150).
By the observed trajectory of mortality, periods with different mortality rates were identified and classified by the nadirs, yielding in the definition of three distinct phases: Phase I from Day 1 until Day 5, phase II from Day 6 until Day 15 and phase III from Day 16 until the end of the observation period at Day 150.
Safety was assessed on the basis of the presence or absence and incidence of AEs and adverse drug reactions (ADRs) reported during the treatment phase until the end of the follow-up observation phase.
Kim, B. J. et al. Phase-sensitive observation of a spin orbital Mott state in Sr2IrO4.
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