Baricitinib for Moderate and Severe Traumatic Intracerebral Hemorrhage/Contusions
报名条件(概要)
- 年龄:18 Years – 80 Years
- 性别:不限
- 健康志愿者:不接受
完整入排标准请以官方页面为准。
开展国家/地区
China
药品与企业信息
其他名称:Baricitinib
Baricitinib with be be administrated orally (or crushed for nasogastric tube delivery) and given daily at the dosage of 4mg for consecutive 14 days
其他名称:Blank control
Patients will receive standard treatment and care according to the current management guidelines for traumatic brain injury.
研发企业
试验官方登记的主要申办方;研究机构申办时会显示相应机构名称。
生产企业
公开药品批准资料或正式说明书暂未提供明确的生产企业信息。
合作机构
- Qianxian People's HospitalUNKNOWN
- Weinan Central Hospital研究机构/其他
- Second Affiliated Hospital of Xi'an Jiaotong University研究机构/其他
- The First Hospital of YulinUNKNOWN
- Xidian Group HospitalUNKNOWN
- Chongqing Emergency Medical Center研究机构/其他
- The Peoples' Hospital of Jiaozuo City研究机构/其他
- First People's Hospital of Xianyang研究机构/其他
- 987th Hospital of the Chinese People's Liberation Army Joint Logistic Support Force研究机构/其他
- Chongqing Hospital of PAPUNKNOWN
- Baoji Fengxiang District HospitalUNKNOWN
- GEM Flower Xian Changqing Staff HospitalUNKNOWN
研发企业与生产企业可能不是同一家。研究阶段药品可能尚未公布生产企业;生产企业仅取自美国上市原研药说明书所列企业(不含仿制药),不作推测;仅在其他国家上市的药品暂无法显示。
研究简介(原文)
The purpose of the present study is to study the effect of baricitinib administration on outcome of participants with moderate and severe traumatic intracerebral hemorrhage/contusions. A multi-center randomized control trial will be conducted. Participants with a radiological diagnosis of traumatic intracerebral hemorrhage/contusions and an initial GCS score of 5-12 will be screened and enrolled in the first 24 hours after traumatic brain injury.
适应症
主动联系研究团队
总联系人(申办方/研究总部)
- Shunnan Ge, M.D,Ph.Dgesn8561@fmmu.edu.cn+8618165295569
中国/港澳台研究中心
- Tandu Hospital, Fourth Military Medical UniversityXi'an,Shaanxi,China
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英文版(发给研究团队)
Dear Study Team, I am a patient in China and I am interested in participating in your clinical trial: Study Title: Baricitinib for Moderate and Severe Traumatic Intracerebral Hemorrhage/Contusions ClinicalTrials.gov Identifier: NCT06065046 Sponsor: Tang-Du Hospital Investigational product: Baricitinib 4 MG, Standard treatment About me: - Age: (please fill in) - Sex: (please fill in) - Confirmed diagnosis and stage: (please fill in) - Biomarkers / genetic testing: not available - Prior and current treatments: (please fill in) - Performance status (ECOG): not assessed - Current location: China - Travel ability: (please fill in) Could you please let me know: 1. Whether I might be eligible for this study; 2. Which site would be closest and most practical for me, and whether remote pre-screening is possible; 3. What documents (medical records, pathology or imaging reports, recent labs) I should prepare for pre-screening. I can provide English translations of my medical records. Thank you very much for your time and help. Kind regards, (your name) (your email / phone with country code)
中文对照(供您核对)
尊敬的研究团队: 我是一位来自中国的患者,希望咨询参加以下临床试验的可能: 研究名称:Baricitinib for Moderate and Severe Traumatic Intracerebral Hemorrhage/Contusions 试验编号:NCT06065046 申办方:Tang-Du Hospital 研究药物:Baricitinib 4 MG、Standard treatment 我的基本情况: - 年龄:(请填写) - 性别:(请填写) - 确诊疾病与分期:(请填写) - 基因/标志物检测:暂无 - 既往及当前治疗:(请填写) - 体能状态(ECOG):未评估 - 目前所在城市:中国 - 可前往范围:(请填写) 想请教三个问题: 1. 我是否可能符合本研究的入组标准? 2. 哪个中心对我最方便可行?能否远程预筛? 3. 预筛需要准备哪些资料(病历、病理、影像、近期化验)? 我可以提供英文翻译版病历。感谢您的时间与帮助。 顺祝安康 (您的姓名) (您的邮箱/带国际区号的电话)
提示:请与主治医生一起发信——由医生署名的申请,回复率远高于患者单独发信。首封邮件不要附身份证号等敏感信息。研究团队通常在 3–10 个工作日内回复,两周无回音可礼貌追问一次。
下一步怎么做?
- 把本页信息带给您的主治医生,评估是否适合参加。
- 点击下方按钮打开官方注册页,查看研究中心联系方式。
- 直接联系研究团队咨询报名事宜(通常有中文同声翻译服务可协助沟通)。