double-blind, clinical trial of the effect of modafinil on cancer-related fatigue among 631 patients receiving chemotherapy: a university of rochester cancer center community clinical oncology program research base study[J]. Cancer, ...
Clinical Trial/Study Report 临床试验/研究报告 A written description of a trial/study of any therapeutic, prophylactic, or diagnostic agent conducted in human subjects, in which the clinical and statistical description, presentations, and analyses are fully integrated into a single report (see the ICH...
In Oracle Clinical and RDC Classic, the term "CRF", which is an acronym for Case Report Form, refers to the form that is used by investigators to collect information and data about a patient in the clinical trial. This form can be either paper or electronic.In...
syn. case record form, data collection form; record of data or other information on subjects in a clinical trial as defined by the protocol ; data may be recorded by hard (e.g. NCR ( no carbon required ) paper) copies, electronic or optical disk methods or any other means, ensuring ...
• Clinical trial/study report 临床试验报告 • COA(药品检测报告) • Co-investigator 合作研究者 • Comparison 对照 • Compliance 依从性 • Computer-assisted trial design ,CATD 计算机辅助试验设计 • Contract research organization ,CRO 合同研究组织 ...
Preview Study CRF Designs in your EDC CRFs are used to collect data from patients during clinical trials. CRF design has a direct impact on the success of clinical trial data as it helps to evaluate the effectiveness of the medical product being trialled. ...
- 《Controlled Clinical Trials》 被引量: 59发表: 2002年 case report form (CRF) syn. case record form, data collection form; record of data or other information on subjects in a clinical trial as defined by the protocol ; data may be recorded by hard (e.g. NCR ( no carbon required ...
NCCN. NCCN clinical practice guidelines in oncology: cancerrelated fatigue (2020)[M]. Version 2. USA: NCCN, 2020: 15. HORNEBER M, FISCHER I, DIMEO F, et al. Cancer-related fatigue: epidemiology, pathogenesis, diagnosis, and treatment [J]. Dtsch Arztebl Int, 2012, 109(9): 161-171; ...
« We chose Medsharing for its reactivity and support level. Medsharing has provided excellent support and rapid turnaround in the development phase of our eCRF so far. » –Dr Stuart L. Silverman, MD FACP FACR, Clinical Professor of Medicine, UCLA School of Medicine and Medical Director,...
, , 6. Without medications in the past two weeks; , , 7. Able to comply with the study and follow-up procedures; , , 8. Written (signed) Informed Consent to participate in the study, and; , , 9. Without participation in any clinical trial within 30 days. A response of NO disquali...