標(biāo)題: Titlebook: Clinical Trials Design in Operative and Non Operative Invasive Procedures; Kamal M.F. Itani,Domenic J. Reda Book 2017 Springer Internation [打印本頁] 作者: 本義 時間: 2025-3-21 17:46
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures影響因子(影響力)
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures影響因子(影響力)學(xué)科排名
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書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures被引頻次
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures被引頻次學(xué)科排名
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures年度引用
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures年度引用學(xué)科排名
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures讀者反饋
書目名稱Clinical Trials Design in Operative and Non Operative Invasive Procedures讀者反饋學(xué)科排名
作者: Torrid 時間: 2025-3-21 22:35
Satellite Communication Systems Designinciple are also discussed. Various cases of practical interest regarding clinical trials for invasive and non-operative procedures are considered. This chapter also outlines other statistical issues that should be taken into consideration in the planning, design, analysis, and interpretation of similar studies.作者: 撕裂皮肉 時間: 2025-3-22 01:21
Introduction to Satellite Communications,re also discussed. Additionally, multiple examples of sample size calculation regarding clinical trials for invasive and nonoperative procedures are detailed along with some conventional guidelines used today in the estimation of sample size.作者: 外貌 時間: 2025-3-22 06:06
Point-of-Care Clinical Trialslinical care ecosystem. A point of care clinical trial of an interventional procedure is presented to demonstrate advantages and limitations of this methodology. This chapter highlights how integration of clinical trials with clinical care serves as a scalable model for healthcare system learning.作者: incredulity 時間: 2025-3-22 09:48
Basic Statistical Considerationsinciple are also discussed. Various cases of practical interest regarding clinical trials for invasive and non-operative procedures are considered. This chapter also outlines other statistical issues that should be taken into consideration in the planning, design, analysis, and interpretation of similar studies.作者: 譏諷 時間: 2025-3-22 13:52
Sample Size Calculationre also discussed. Additionally, multiple examples of sample size calculation regarding clinical trials for invasive and nonoperative procedures are detailed along with some conventional guidelines used today in the estimation of sample size.作者: 譏諷 時間: 2025-3-22 17:48 作者: Dri727 時間: 2025-3-23 00:44 作者: 破布 時間: 2025-3-23 05:07
The Research Question and the Hypothesis primary hypothesis to be tested, needs to set the steps in motion to define the research methodology and analytic plan for the trial, needs to be answerable, and ultimately needs to offer promise that this answer will provide critical new knowledge that will change clinical practice for the better and improve patient outcomes.作者: 決定性 時間: 2025-3-23 08:05 作者: Coronary-Spasm 時間: 2025-3-23 10:14 作者: Spina-Bifida 時間: 2025-3-23 16:55
https://doi.org/10.1007/978-3-642-18861-9 primary hypothesis to be tested, needs to set the steps in motion to define the research methodology and analytic plan for the trial, needs to be answerable, and ultimately needs to offer promise that this answer will provide critical new knowledge that will change clinical practice for the better and improve patient outcomes.作者: 有法律效應(yīng) 時間: 2025-3-23 18:32 作者: 取回 時間: 2025-3-23 23:37 作者: GRATE 時間: 2025-3-24 05:49
Book 2017 with industry.?.Clinical Trials Design in Invasive Operative and Non Operative Procedures. will be of interest to?all specialists of surgery, anesthesiologists, interventional radiologists, gastroenterologists, cardiologists, and pulmonologists.作者: follicle 時間: 2025-3-24 08:14
https://doi.org/10.1007/BFb0117924front, but allow the investigator to dig more deeply into the more subtle information provided by the trial that may or may not provide definitive conclusions, but might dictate the direction of future studies.作者: Crohns-disease 時間: 2025-3-24 11:42 作者: 貿(mào)易 時間: 2025-3-24 16:23
Primary and Secondary Endpointsfront, but allow the investigator to dig more deeply into the more subtle information provided by the trial that may or may not provide definitive conclusions, but might dictate the direction of future studies.作者: 可用 時間: 2025-3-24 22:07 作者: 倫理學(xué) 時間: 2025-3-25 02:47 作者: 坦白 時間: 2025-3-25 05:32 作者: ARM 時間: 2025-3-25 08:50 作者: 偽造者 時間: 2025-3-25 11:53 作者: ethnology 時間: 2025-3-25 19:42
Pragmatic Trialstudy. Pragmatically designed trials have a host of limitations that are often underappreciated, and extrapolating results can drive harmful policies. Care should be taken in interpretation of pragmatic trials. In this chapter, we define a pragmatic trial; we discuss key design and analytic features 作者: Panacea 時間: 2025-3-25 20:38 作者: Hemoptysis 時間: 2025-3-26 04:02
equirements, and adjuncts to clinical trials and interaction with industry.?.Clinical Trials Design in Invasive Operative and Non Operative Procedures. will be of interest to?all specialists of surgery, anesthesiologists, interventional radiologists, gastroenterologists, cardiologists, and pulmonologists.978-3-319-85263-8978-3-319-53877-8作者: 輕率的你 時間: 2025-3-26 04:31
G. K. Hartmann,K. Oberl?nder,J. P. Sch?del standard, especially if it incurs greater risk. Finally, the proper control group needs to be selected to make the comparison and conclusions believable, applicable, and generalizable. If these criteria are reached, then you are another step closer to the critical new knowledge that will positively作者: 安慰 時間: 2025-3-26 09:18 作者: 礦石 時間: 2025-3-26 13:14 作者: avarice 時間: 2025-3-26 20:22 作者: Dappled 時間: 2025-3-27 00:16
https://doi.org/10.1007/978-1-4615-3006-0tudy. Pragmatically designed trials have a host of limitations that are often underappreciated, and extrapolating results can drive harmful policies. Care should be taken in interpretation of pragmatic trials. In this chapter, we define a pragmatic trial; we discuss key design and analytic features 作者: 出沒 時間: 2025-3-27 03:44 作者: 下級 時間: 2025-3-27 06:43
Clinical Trials Design in Operative and Non Operative Invasive Procedures作者: 行為 時間: 2025-3-27 12:30
Clinical Trials Design in Operative and Non Operative Invasive Procedures978-3-319-53877-8作者: GROUP 時間: 2025-3-27 17:19
Clinical Phases of Device and Drug Evaluation with Emphasis on Early Phase Trialsscribing them in depth. This chapter discusses the various types of trials defined by regulatory agencies that are required to move a drug, vaccine, biologic or devices that carry significant risk from preclinical testing to marketing approval. This chapter focuses specifically on early phase trials.作者: 仔細(xì)檢查 時間: 2025-3-27 19:17
Kamal M.F. Itani,Domenic J. RedaProvides the framework for building a clinical trial as it pertains to operative and non operative invasive procedures.Written by experts in the field.Provides details of building a scientifically and作者: 盡管 時間: 2025-3-28 00:50 作者: 惡心 時間: 2025-3-28 04:15 作者: 采納 時間: 2025-3-28 07:55 作者: 音樂戲劇 時間: 2025-3-28 11:07 作者: 反復(fù)無常 時間: 2025-3-28 15:16 作者: 碳水化合物 時間: 2025-3-28 20:09
https://doi.org/10.1007/978-3-642-18861-9p front is as valuable as the time that will be spent conducting the trial itself. Start simple with real ideas that are meaningful to your clinical practice and specialty. Refine your ideas into a more defined research question. This research question needs to be relevant, needs to translate to the作者: 頑固 時間: 2025-3-29 00:42
https://doi.org/10.1007/BFb0117924 associated with the primary research question and hypothesis and therefore is the main outcome of the study. For this reason, it needs to be well defined in advance and needs to be easily measurable with tools that are ideally readily available, simple to use, accurate, and validated. The closer an作者: CHURL 時間: 2025-3-29 06:49 作者: Occupation 時間: 2025-3-29 10:19 作者: canonical 時間: 2025-3-29 11:38
Frequency and Propagation Considerations,scribing them in depth. This chapter discusses the various types of trials defined by regulatory agencies that are required to move a drug, vaccine, biologic or devices that carry significant risk from preclinical testing to marketing approval. This chapter focuses specifically on early phase trials作者: sinoatrial-node 時間: 2025-3-29 15:45
Non-Geostationary Orbit Satellite Systems,the specific medical condition of interest. The advent of the RCT is relatively recent, with the first major trial reporting results shortly after World War II. However, the various design elements that provide the rigor of the RCT had developed over hundreds of years. In fact, the basic idea of lea作者: 陶醉 時間: 2025-3-29 19:58
Orbits and Controlled Trajectories,ation with the other treatment(s). Thus, it can be a very efficient design to answer multiple questions about the various treatments. A key issue in the design and interpretation of results for a factorial design is that of effect modification, or treatment interaction. When interaction exists betwe作者: 勤勞 時間: 2025-3-30 00:59
Satellite Communication Systems Designroup trial. It has two main advantages. The first being increased precision which allows a reduction in the required sample size, often dramatic, compared with a parallel-group trial. The second advantage is that it may enhance recruitment as each study participant will receive an active treatment i作者: Inexorable 時間: 2025-3-30 06:19
https://doi.org/10.1007/978-1-4615-3006-0propriately applied at a group level (e.g., provider, clinic, hospital). Since patients within a provider, clinic, or hospital are more likely to be similar than patients from another provider, clinic, or hospital, this correlation, called the intraclass correlation (ICC), must be accounted for in t作者: Soliloquy 時間: 2025-3-30 11:39 作者: committed 時間: 2025-3-30 14:57
https://doi.org/10.1007/978-1-4615-3006-0omparative effectiveness studies is needed to improve health-care quality and to support the efficient use of limited resources. Pragmatic trials are a type of experimental comparative effectiveness research that are designed to determine the effects of an intervention under the usual condition(s) i作者: mutineer 時間: 2025-3-30 18:11 作者: ornithology 時間: 2025-3-30 21:22 作者: CHYME 時間: 2025-3-31 02:29 作者: 拱形大橋 時間: 2025-3-31 08:35
Introduction to Satellite Communications,ving invasive operative and nonoperative procedures. It focuses on the key elements for sample size determination that includes acquiring a reliable estimate of the treatment effect and variability, the type of endpoint to be analyzed, treatment allocation, and expected recruitment and retention rat作者: Incorporate 時間: 2025-3-31 12:18
Frequency and Propagation Considerations,scribing them in depth. This chapter discusses the various types of trials defined by regulatory agencies that are required to move a drug, vaccine, biologic or devices that carry significant risk from preclinical testing to marketing approval. This chapter focuses specifically on early phase trials.作者: motivate 時間: 2025-3-31 16:54 作者: 先行 時間: 2025-3-31 19:26
Primary and Secondary Endpoints associated with the primary research question and hypothesis and therefore is the main outcome of the study. For this reason, it needs to be well defined in advance and needs to be easily measurable with tools that are ideally readily available, simple to use, accurate, and validated. The closer an作者: 矛盾心理 時間: 2025-4-1 00:57
