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The present study was designed to assess the antithrombotic effect of both dual antiplatelet regimens using a human ex vivo model of arterial thrombosis.
Patients were subsequently randomly allocated to one of the three treatment regimens using a simple randomization procedure (shuffled deck of cards) (Table 1).
Current guidelines for the treatment of patients with advanced NSCLC recommend platinum-based combination regimens using a third-generation agent as first-line treatment [ 3- 5].
This study compared the efficacy and safety of once-daily (OD) and twice-daily (BID) glycopyrronium bromide regimens, using a novel model-based approach, in patients with moderate-to-severe COPD.
Survival results were combined for each pre-specified category of regimens using a random-effects model, and meta-regression models were used to adjust for heterogeneity in some known prognostic factors.
In the present study, we report for the first time, the distribution of 4OHtam, 4OHNDtam, and tamNox in breast cancer tissue during normal- and two low-dose regimens using a highly sensitive HPLC-MS/MS assay.
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The largest magnitude HCV-specific T-cell responses seen in animal models and humans have come from regimens using Ad vectors.
Table 4 shows logistic regression results for both clinical regimens using an outcome of blood loss ≥ 700 mL.
ClinicalTrials.gov Identifier NCT00703898 Currently, the preferred first-line antiretroviral regimens use a combination of two nucleoside reverse transcriptase inhibitors (NRTIs) and either a non-nucleoside reverse transcriptase inhibitor (NNRTI) or a ritonavir-boosted protease inhibitor [ 1].
Study Objectives: To compare patients' functional ability in the 24-hour postoperative period following a remifentanil compared to a hypnotic-fentanyl-treated anesthesia regimen using a 24-Hour Functional Ability Questionnaire.
STUDY OBJECTIVES: To compare patients' functional ability in the 24-hour postoperative period following a remifentanil compared to a hypnotic-fentanyl-treated anesthesia regimen using a 24-Hour Functional Ability Questionnaire.
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