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注册号: Registration number: |
ChiCTR2500099758 |
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最近更新日期: Date of Last Refreshed on: |
2025-03-28 08:51:28 |
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注册时间: Date of Registration: |
2025-03-28 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
术中持续雾化吸入艾司氯胺酮对老年腹腔镜结直肠癌根治术患者的肺保护作用研究 |
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Public title: |
The pulmonary protective effect of continuous inhalation of esketamine in elderly patients undergoing laparoscopic radical resection of colorectal cancer |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
术中持续雾化吸入艾司氯胺酮对老年腹腔镜结直肠癌根治术患者的肺保护作用研究 |
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Scientific title: |
The pulmonary protective effect of continuous inhalation of esketamine in elderly patients undergoing laparoscopic radical resection of colorectal cancer |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
蔡雪姣 |
研究负责人: |
姚雷 |
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Applicant: |
Xuejiao Cai |
Study leader: |
Lei Yao |
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申请注册联系人电话: Applicant telephone: |
+86 183 6219 7225 |
研究负责人电话:
Study leader's |
+86 188 6292 0110 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
1532451090@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
yaoleijiangsu1987@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
江苏省南通市崇川区胜利路666号 |
研究负责人通讯地址: |
江苏省南通市崇川区胜利路666号 |
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Applicant address: |
No. 666, Shengli Road, Chongchuan District, Nantong City, Jiangsu Province |
Study leader's address: |
No. 666, Shengli Road, Chongchuan District, Nantong City, Jiangsu Province |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
南通大学第二附属医院 |
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Applicant's institution: |
The Second Affiliated Hospital of Nantong University |
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研究负责人所在单位: |
南通市第一人民医院 |
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Affiliation of the Leader: |
Nantong First People's Hispital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2025XM111 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
南通市第一人民医院伦理委员会 |
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Name of the ethic committee: |
Nantong First People's Hispital Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-02-25 00:00:00 | ||
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伦理委员会联系人: |
徐红青 |
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Contact Name of the ethic committee: |
Hongqing Xu |
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伦理委员会联系地址: |
江苏省南通市崇川区胜利路666号 |
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Contact Address of the ethic committee: |
No. 666, Shengli Road, Chongchuan District, Nantong City, Jiangsu Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 159 5131 2678 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
南通市第一人民医院 |
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Primary sponsor: |
Nantong First People's Hispital |
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研究实施负责(组长)单位地址: |
江苏省南通市崇川区胜利路666号 |
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Primary sponsor's address: |
No. 666, Shengli Road, Chongchuan District, Nantong City, Jiangsu Province |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
南通市第一人民医院 |
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Source(s) of funding: |
Nantong First People's Hispital |
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研究疾病: |
术后肺部并发症 |
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Target disease: |
Postoperative pulmonary complications |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
通过比较术中持续雾化吸入艾司氯胺酮与静脉持续输注艾司氯胺酮在老年腹腔镜结直肠癌根治术患者中的效果,分析其对血药浓度、呼吸功能、呼吸力学参数、血清炎性因子水平、术后疼痛、术后肺部并发症(PPCs)。等的影响。从而明确术中持续雾化吸入艾司氯胺酮在老年腹腔镜结直肠癌根治术中的肺保护作用,并深入探讨其潜在的作。用机制与途径。期望能优化患者的肺功能,减少PPCs发生,改善术后疼痛,并评估雾化吸入途径相较于同期静脉输注是否具有优势 |
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Objectives of Study: |
Compared the effects of continuous inhalation of esketamine and continuous intravenous infusion of esketamine in elderly patients undergoing laparoscopic radical resection of colorectal cancer and to analyze its effects on blood drug concentration, respiratory function, respiratory mechanical parameters, serum inflammatory factor levels, postoperative pain and postoperative pulmonary complications (PPCs). In order to clarify the pulmonary protection effect of continuous inhalation of esketamine in elderly patients undergoing laparoscopic radical resection of colorectal cancer, and explore its potential mechanism and pathway. It is expected to optimize lung function, reduce the occurrence of PPCs, improve postoperative pain, and evaluate the advantages of nebulizing over concurrent intravenous infusion. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1.合并严重心脑血管疾病者; 2.合并严重肝肾功能障碍者; 3.术前肺功能测定值低于预计值65%者; 4.长期阿片类药物使用者; 5.肺部感染或全身感染患者; 6.近期使用抗炎药物或抗氧化药物者; 7.长期使用糖皮质激素或免疫抑制剂者; 8.对艾司氯胺酮过敏史或者有使用禁忌症有血压和颅内压升高严重风险、控制不佳或者未经治疗的高血压、未经治疗或者治疗不足的甲状腺功能亢进、有消化道出血.; 9.有精神疾病和其他慢性疼痛或其他可能混淆镇痛反应的情况; 10.急诊手术或创伤患者; 11.既往有腹部手术或术中知晓史。 |
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Exclusion criteria: |
1. Patients with severe cardiovascular and cerebrovascular diseases; 2. Patients with severe liver and kidney dysfunction; 3. The preoperative pulmonary function test value is lower than 65% of the predicted value; 4. Long-term opioid users; 5. Patients with lung infection or systemic infection; 6. Those who have recently used anti-inflammatory drugs or antioxidant drugs; 7. Long-term use of glucocorticoids or immunosuppressants; 8. History of allergy to esketamine or contraindications to use, serious risk of elevated blood pressure and intracranial pressure, poorly controlled or untreated hypertension, untreated or undertreated hyperthyroidism, gastrointestinal bleeding.; 9. Have psychiatric illness and other chronic pain or other conditions that may confound analgesic responses; 10. Emergency surgery or trauma patients; 11. Previous abdominal surgery or intraoperative history. |
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研究实施时间: Study execute time: |
从 From 2025-02-08 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-04-01 00:00:00 至 To 2026-11-30 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
利用统计软件按随机化方法生成随机数字表,之后将随机分组结果密封于不透光的信封内,筛选入组患者时,按照信封内的分组结果进入相应的试验组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Using statistical software, a random number table was generated through a randomization method. The randomized grouping results were then sealed in opaque envelopes. During patient screening and enrollment, participants were assigned to the corresponding trial groups based on the grouping results contained within the envelopes. |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
双盲:实验对象,实验人员 |
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Blinding: |
Double-blind:subjects,researchers |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
有兴趣者可向作者要求共享原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Anyone interested in the trial can ask authors for sharing the IPD. |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
数据记录表,Excel电子数据表,运用SPSS软件进行统计分析 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data record from and Excel database for data collection and SPSS for statistical analysis. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |