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注册号: Registration number: |
ChiCTR2100051521 |
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最近更新日期: Date of Last Refreshed on: |
2022-04-12 15:26:59 |
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注册时间: Date of Registration: |
2021-09-25 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: |
请与我们联系上传伦理审批文件。 超声引导PNGB联合LFCNB对比FICB对全髋关节置换术后镇痛及运动功能影响的研究 |
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Public title: |
Ultrasonic guidance PNGB combined with LFCNB to compare the effects of ficb on the pain and motion function of total hip replacement |
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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: |
超声引导PENGB联合LFCNB对全髋关节置换术后运动功能的影响 |
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Scientific title: |
Effect of ultrasound-guided PENGB combined with LFCNB on motor function after total hip arthroplasty |
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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: |
梁露丹 |
研究负责人: |
何开华 |
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Applicant: |
Liang Ludan |
Study leader: |
He Kaihua |
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申请注册联系人电话: Applicant telephone: |
+86 17748090862 |
研究负责人电话:
Study leader's |
+86 13908396469 |
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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: |
ludaaan@163.com |
研究负责人电子邮件: Study leader's E-mail: |
13908396469@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: |
重庆市渝中区友谊路1号 |
研究负责人通讯地址: |
重庆市渝中区友谊路1号 |
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Applicant address: |
1 Youyi Road, Yuzhong District, Chongqing, China |
Study leader's address: |
1 Youyi Road, Yuzhong District, Chongqing, China |
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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: |
重庆医科大学附属第一医院麻醉科 |
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Applicant's institution: |
Department of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University |
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研究负责人所在单位: |
重庆医科大学附属第一医院麻醉科 |
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Affiliation of the Leader: |
Department of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University |
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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: |
2021-316 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
重庆医科大学附属第一医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Chongqing Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
1990-01-01 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
重庆市渝中区友谊路1号 |
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Contact Address of the ethic committee: |
1 Youyi Road, Yuzhong District, Chongqing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
重庆医科大学附属第一医院麻醉科 |
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Primary sponsor: |
Department of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University |
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研究实施负责(组长)单位地址: |
重庆市渝中区友谊路1号 |
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Primary sponsor's address: |
1 Youyi Road, Yuzhong District, Chongqing, China |
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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: |
自筹 |
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Source(s) of funding: |
Self-raised |
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研究疾病: |
股骨头坏死;髋关节骨折 |
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Target disease: |
Necrosis of femoral head; Hip fracture |
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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: |
I期临床试验 | ||||||||||||||||||||||
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Study phase: |
1 |
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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: |
比较髋关节囊周围神经阻滞(PNGB)联合股外侧皮神经阻滞(LFCNB) 与髂筋膜间隙阻滞(FICB)在全髋关节置换术患者的术后镇痛效果差异,以及对运动功能的影响;寻找对全髋关节置换术患者术后镇痛效果更好,运动功能影响更小的神经阻滞方法。 |
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Objectives of Study: |
To compare the postoperative analgesic effect of hip joint peripheral nerve block (PNGB) combined with lateral femoral cutaneous nerve block (LFCNB) and fascia iliaca space block (FICB) in patients with total hip arthroplasty, as well as on motor function To find a nerve block method with better postoperative analgesia and less impact on motor function in patients undergoing total hip arthroplasty. |
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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: |
精神病患者;穿刺点局部皮肤感染;外周神经病变;凝血功能障碍;阿片类药物滥用;慢性疼痛;无法配合行视觉模拟评分(VAS)者;药物无法控制的高血压患者;其他无法耐受本实验的患者。 |
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Exclusion criteria: |
A psychopath; Local skin infection at puncture site; Peripheral neuropathy; Coagulation dysfunction; Opioid abuse; Chronic pain; Unable to match the visual analog scale (VAS); Patients with hypertension that cannot be controlled by drugs; Other patients who could not tolerate the study. |
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研究实施时间: Study execute time: |
从 From 2021-10-01 00:00:00至 To 2022-10-15 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-10-01 00:00:00 至 To 2022-10-01 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: |
正在进行 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): |
研究者使用计算机软件对受试者进行随机化分配。患者入选后,手术前由ResMan信息系统产生随机数字并进行随机分组,同时产生受试者编号。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The researchers used computer software to randomize the subjects. After the patients were enrolled, the ResMan information system generated random numbers and randomly grouped them before surgery, and the subject numbers were generated at the same time. |
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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: |
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Blinding: |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
no |
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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: |
Excel,SPSS |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Excel,SPSS |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |