Sun Wenwu, Zhao Bing, Li Jiaoyan, Wang Yihui, Qi Xing, Ning Ning, Sun Silei, Li Mengjiao, Yao Yi, Ni Tongtian, Ma Li, He Juan, Huang Jun, Yang Zhitao, Chen Ying, Sheng Huiqiu, Mao Enqiang
Department of Emergency, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Pharmacy, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Front Med (Lausanne). 2023 Nov 9;10:1278167. doi: 10.3389/fmed.2023.1278167. eCollection 2023.
Acute pancreatitis is a common gastrointestinal disease. The mortality of patients affected by severe acute pancreatitis (SAP) remains high. It is unclear whether high-dose intravenous vitamin C (HDIVC) therapy could improve the prognosis of these patients. The current prospective, randomized, double-blinded, placebo-controlled study will explore the effect of high-dose intravenous vitamin C therapy on the prognosis in patients with moderately severe and severe acute pancreatitis.
A total of 418 participants with moderately severe and severe acute pancreatitis who meet the eligible criteria will be randomly assigned in a 1:1 ratio to receive treatment with HDIVC (200 mg/kg/24 h) or placebo (saline) for a period of 7 days. The primary outcome is 28-day mortality in these patients. The secondary outcomes include organ functions and interventions, laboratory tests, healthcare, and 90-day mortality.
This protocol was approved by the institutional ethics board of the Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China (Registration Number: 2019-90). The report of the study will be published in peer-reviewed journals and presented at conferences, both nationally and internationally.
Chinese Clinical Trial Registry (ChiCTR1900022022). Version 1.5.
急性胰腺炎是一种常见的胃肠道疾病。重症急性胰腺炎(SAP)患者的死亡率仍然很高。大剂量静脉注射维生素C(HDIVC)疗法是否能改善这些患者的预后尚不清楚。当前这项前瞻性、随机、双盲、安慰剂对照研究将探讨大剂量静脉注射维生素C疗法对中度和重度急性胰腺炎患者预后的影响。
共有418名符合入选标准的中度和重度急性胰腺炎参与者将按1:1的比例随机分配,接受HDIVC(200mg/kg/24小时)或安慰剂(生理盐水)治疗7天。主要结局是这些患者的28天死亡率。次要结局包括器官功能和干预措施、实验室检查、医疗保健以及90天死亡率。
本方案已获得中国上海交通大学医学院附属瑞金医院机构伦理委员会的批准(注册号:2019 - 90)。该研究报告将发表在同行评审期刊上,并在国内和国际会议上展示。
中国临床试验注册中心(ChiCTR1900022022)。版本1.5