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Study Design and Setting: Two separate prospective, matched, nonrandomized, open enrollment treatment groups (RFTVR, n = 73 and nasal continuous positive airway pressure (CPAP, n = 99) were concurrently enrolled in a multicenter study.
We used data of 1359 patients with LRTI enrolled in a multicenter study.
In patients with ALI/ARDS enrolled in a multicenter study of a protective ventilatory strategy, higher baseline levels of IL-6 and IL-8 were associated with increased mortality [ 5].
A total of 1354 older diabetic in-patients consecutively enrolled in a multicenter study formed the training population (retrospective arm); 264 patients consecutively admitted to a ward of general medicine formed the testing population (prospective arm).
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Children aged ≤16 years with clinical and radiological pneumonia were enrolled in a multicenter prospective study.
Detailed clinical data and sera from 963 patients with SSc enrolled in a multicenter cohort study were collected and entered into a central database.
Subjects with moderate to severe COPD enrolled in a multicenter, randomized controlled study (NCT00857766) were included.
Data were collected from a cohort of 202 patients (84 men) enrolled in a multicenter prospective registry study of PE.
It is important to note that while this study utilized a cohort of patients enrolled in a multicenter, high-dose therapy trial, our primary study question was not related to high-dose therapy.
The objective of the study was to compare the efficacy and safety of frovatriptan and almotriptan in women with menstrually related migraine (IHS Classification of Headache disorders) enrolled in a multicenter, randomized, double-blind, cross-over study.
To compare the efficacy and safety of frovatriptan and almotriptan in women with menstrually related migraine (IHS Classification of Headache disorders) enrolled in a multicenter, randomized, double blind, cross-over study.
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