完成了PRS账号申请,打开 ClincialTrial.gov登录界面,如图2所示,在输入单位信息, 用户名和密码,进入临床试验注册的界面。建议初学者要严格按照流程,一步步认真填写ClincialTrial.gov中研究方案的信息,在需要填写的内容涵盖了临床试验的方面,包括研究方案与背景资料,受试者评审信息和FDA相关12个方面内容。ClinicalTrial.gov...
试验目的 Clinical trial participation has always been substantially skewed toward certain demographic groups. However, there has been little study on whether trial qualities impact participation in either a positive or negative way. The goal of this research is to identify the characteristics that consis...
ClinicalTrials数据库提供临床试验Novel Combination Therapy for Osteoporosis in Men的登记号NCT03994172,试验分期Phase 4以及申办者VA Office of Research and Development的信息,更过关于临床试验的其他信息查询就在戊戌数据美国临床试验数据库.
试验目的 Clinical trial participation has always been substantially skewed toward certain demographic groups. However, there has been little study on whether trial qualities impact participation in either a positive or negative way. The goal of this research is to identify the characteristics that consis...
The objective of this study is to determine if tAN therapy can reduce the median number of days of oral morphine administered to an infant after start of treatment. 详细描述 This study is designed as a randomized, double-blind, sham-controlled, multi-center, clinical trial in which neonates...
Secondary outcomes are self-reported health-related quality of life, general self-efficacy and the number of acute visits to the orthopaedic outpatient clinic. Discussion The result of this trial is expected to provide new knowledge to support the development of targeted and effective follow-up ...
The trial is coordinated by the Coordinating Center for Clinical Trials in cooperation with BBraun Aesculap. Both were responsible for management and registration (Identifier Number NCT 0005725079, http://www.clinicaltrials.gov) and all trial related meetings. The trial is performed according to the...
The investigator explained the study to each patient, covering the following points: (1) objectives and methods of the study; (2) scheduled participation period and planned number of participants; (3) anticipated clinical benefits and risks; (4) each patient is free to refuse to participate in...
SOLIDARITY Finland (Plus) is an adaptive, randomized, open-label clinical trial evaluating the safety and efficacy of imatinib, infliximab, and local standard of care in hospitalized adult patients diagnosed with COVID-19.) Study population: The study population consists of adult patients (18 years...
A larger negative value indicates a better overall clinical outcome. The Usage of Rescue Medication (Acetaminophen/Paracetamol) at 26 Weeks [ TimeFrame: 26 Weeks ] The usage of Rescue Medication (RM) as based on the average number of acetominophen/paracetamol pills taken among participants ...