Pooling the hazard ratios is not always feasible in meta-analyses of two-arm survival studies, because the measure of the intervention effect is not system... Combescure,Courvoisier,S D.,... 被引量: 0发表: 0年 Prospective Randomized Two-Arm Controlled Study To Determine the Efficacy of a ...
2. 双组 ...ozogamicin的一项III期随机、开放标签、双组(two-arm)研究(B1931008),该项研究在不适合高剂量化疗的复发性或难治 … www.bioon.com|基于3个网页 3. 两个组 简介:辉瑞将终止有关实验性药物inotuzumab ozogamicin的一项III期随机、开放标签、两个组(two-arm)研究(B1931008内 … ...
Viral infections remain a major risk in immunocompromised pediatric patients, and virus-specific T cell (VST) therapy has been successful for treatment of refractory viral infections in prior studies. We performed a phase II multicenter study (NCT0347521
In this paper, we present the architecture of an experimental real-time control system called TRACS (two robotic arm coordination system) and experimental results using two PUMA 250 robot arms that perform tasks of manipulating large objects. The system uses an IBM PC-AT as the host computer wh...
monitors being the mirror version of each other along the vertical axis. The motivation behind the presentation of such paired visual scenes was to show to the rats the same visual stimulus, regardless of the arm from which it would inspect the monitors. In fact, in this design, the arm wh...
This study evaluates the effect of progressive nicotine reduction in cigarettes on smoking behavior, toxicant exposure, and psychiatric symptoms in smokers with comorbid mood and/or anxiety disorders using a two-site, two-arm, double-blind, parallel group, randomized controlled trial (RCT) in four ...
26and main findings have been published27,28. The marine n-3 arm results for the cognitive substudies have been analyzed separately59. Participants We used data from two distinct subsets of VITAL participants. Although cognitive function was not the main planned outcome to be evaluated in the ...
MEDITAGING is a two-arm randomized, double-blinded, controlled study, which will include older Portuguese-speaking migrants (n = 90). Participants are randomized to the MBSR or a health promotion program. Both interventions are conducted in groups over a total of 8 weeks, incorporating week...
SmartPill as an objective parameter for determination of severity and duration of postoperative ileus: study protocol of a prospective, two-arm, open-label... SmartPill(R) as an objective parameter for determination of severity and duration of postoperative ileus: study protocol of a prospective, ...
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