Study protocol: a prospective controlled clinical trial to assess surgical or medical treatment for paediatric type 2 diabetes (ST 2 OMP)paediatric endocrinologypaediatric surgerylipid disordersIntroduction The pathophysiology of type 2 diabetes (T2D) in youth differs from adults and conventional medical ...
Study protocols reporting a clinical trial can be formatted for submission toTrialsin two ways: By following the guidance set out in ourstructured study protocol template. This is the preferred option if you have not yet started writing your manuscript. ...
◆CTP临床试验方案 (Clinical Trial Protocol):指说明临床试验目的、设计、方法学、统计学考虑和组织实施的文件。试验方案通常还应当包括临床试验的背景和理论基础,该内容也可以在其他参考文件中给出。试验方案包括方案及其修订版。 ◆SOP标准操作规程 (Standard Operating Procedure):指为保证某项特定操作的一致性而制定...
Study protocol of a phase 1 clinical trial establishing the safety of intrapleural administration of liposomal curcumin: curcumin as a palliative treatment... Introduction This is a phase 1, open-label, single-centre, uncontrolled, dose-escalation study to evaluate the feasibility, tolerability and ...
相关知识点: 试题来源: 解析 PreCardio-study protocol 心前区研究协议The PreCardio-study protocol – a randomized clinical trial of a multidisciplinary electronic cardiovascular prevention programme心前区研究协议-- 跨学科电子心血...反馈 收藏
optimizing clinical trials from concept to conclusion: from study and protocol design, trial planning and budgeting, site negotiation, [...] mdsol.com Medidata公司先进的平台从构想到实现全方位优化临床试验来降低临床开发的总成本: 从 研 究 和方 案设 计、试验规划和预算、 研 究 单位 谈判 、临...
MDMA-assisted Psychotherapy in Chronic PTSD 9/24/03, revised 5/16/06 0 Principal Investigator: Michael C Mithoefer. Sponsor: MAPS Study Protocol Phase II clinical trial testing the safety and efficacy of 3,4- methylenedioxymethamphetamine (MDMA)-assisted psychotherapy in subjects with chronic posttr...
Study protocol: a randomized clinical trial of total parenteral nutrition in malnourished surgical patients. CSP #221 is a randomized multiinstitutional clinical trial to assess the efficacy of 10 d of perioperative total parenteral nutrition (TPN) in reducing mor... GP Buzby,LS Knox,LO Crosby,....
The results will be submitted to ClinicalTrials.gov via the Protocol Registration and Results System Information Website. Informed consent will have a specific statement informing participants that results from the study will be posted on ClincalTrials.gov. ...
The clinical trial is ongoing. The recruitment started in January 2022. There are no practical or operational issues involved in performing the study. Trial status This is version 2.2 of the protocol, written on January 20, 2022. The recruitment started in January 26 2022, directly after approva...