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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2500106810 |
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最近更新日期: Date of Last Refreshed on: |
2025-07-30 15:59:18 |
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注册时间: Date of Registration: |
2025-07-30 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: |
环乳晕入路乳房上提内旋固定Ⅰ期假体植入纠正轻度乳房下垂的疗效研究 |
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Public title: |
A Study on the Efficacy of Periareolar Approach Breast Lift with Internal Rotation Fixation and Stage I Implant Placement for Correcting Mild Breast Ptosis |
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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: |
环乳晕入路乳房上提内旋固定Ⅰ期假体植入纠正轻度乳房下垂的疗效研究 |
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Scientific title: |
A Study on the Efficacy of Periareolar Approach Breast Lift with Internal Rotation Fixation and Stage I Implant Placement for Correcting Mild Breast Ptosis |
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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: |
周笑梅 |
研究负责人: |
吴毅平 |
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Applicant: |
Xiaomei Zhou |
Study leader: |
Yiping Wu |
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申请注册联系人电话: Applicant telephone: |
+86 158 7160 8829 |
研究负责人电话:
Study leader's |
+86 139 8607 2558 |
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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: |
413723358@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
413723358@qq.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
华中科技大学 |
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: |
湖北省武汉市硚口区解放大道1095号 |
研究负责人通讯地址: |
湖北省武汉市硚口区解放大道1095号 |
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Applicant address: |
No. 1095, Jiefang Avenue, Qiaokou District, Wuhan City, Hubei Province |
Study leader's address: |
No. 1095, Jiefang Avenue, Qiaokou District, Wuhan City, Hubei Province |
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申请注册联系人邮政编码: Applicant postcode: |
441800 |
研究负责人邮政编码: Study leader's postcode: |
441800 |
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申请人所在单位: |
华中科技大学同济医学院附属同济医院 |
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Applicant's institution: |
Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology |
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研究负责人所在单位: |
华中科技大学同济医学院附属同济医院 |
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Affiliation of the Leader: |
Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology |
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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: |
TJ-IRB202506072 |
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: |
华中科技大学同济医学院附属同济医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-06-26 00:00:00 | ||
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伦理委员会联系人: |
华中科技大学同济医学院附属同济医院医学伦理委员会 |
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Contact Name of the ethic committee: |
Medical Ethics Committee of Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology |
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伦理委员会联系地址: |
湖北省武汉市解放大道1095号 |
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Contact Address of the ethic committee: |
No. 1095, Jiefang Avenue, Wuhan City, Hubei Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 27 8366 2379 |
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: |
华中科技大学同济医学院附属同济医院 |
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Primary sponsor: |
Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology |
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研究实施负责(组长)单位地址: |
湖北省武汉市硚口区解放大道1095号 |
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Primary sponsor's address: |
No. 1095, Jiefang Avenue, Qiaokou District, Wuhan City, Hubei 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: |
同济医院高质量临床研究基金 |
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Source(s) of funding: |
Tongji Hospital Clinical Research Fund |
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研究疾病: |
乳房下垂 |
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Target disease: |
Breast sagging |
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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: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
本研究旨在通过对术前、术后主要乳房径线数据的分析,评估乳房下垂改善的程度,评价PAM-WU-Ⅰ用于改善轻度乳房下垂的有效性与安全性,为改善乳房下垂提供更多的治疗方案及科学依据。 |
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Objectives of Study: |
This study aims to assess the degree of improvement in breast ptosis by analysing pre- and post-operative data on key breast dimensions, evaluate the efficacy and safety of PAM-WU-Ⅰ in improving mild breast ptosis, and provide additional treatment options and scientific evidence for improving breast ptosis. |
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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: |
患者年龄>=18 岁且<60 岁女性;经体表测量乳头上提距离小于5cm的轻度乳房松垂患者。受试者理解并能配合本研究;根据乳房整形操作指南,患者将在此次手术中获益。 |
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Inclusion criteria |
Female patients aged >=18 years and <60 years; patients with mild breast ptosis as determined by measuring the distance from the nipple to the skin surface, which is less than 5 cm. Participants must understand and be able to cooperate with this study; according to the guidelines for breast augmentation surgery, patients are expected to benefit from this procedure. |
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排除标准: |
乳腺肿瘤病史患者,术前影像学/穿刺证实合并乳房肿瘤患者;受试者需接受其他乳房手术等;根据美国麻醉医师协会评分(ASA)大于 4 分,存在高度手术风险者;由评估小组术前根据乳房影像资料评估乳房部分缺损,术中需联合皮瓣修复或NAC 再造的患者;合并精神心理疾病患者;合并严重基础性疾病患者;孕期、哺乳期;胸廓有明显的倾斜畸形,如漏斗胸、鸡胸;个人意愿排斥该手术患者,既往已行乳房整形手术(假体植入/下垂矫正/自体脂肪移植等)患者。 |
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Exclusion criteria: |
Patients with a history of breast tumours, confirmed by preoperative imaging/biopsy to have concurrent breast tumours; subjects requiring other breast surgeries; patients with an American Society of Anaesthesiologists (ASA) score greater than 4, indicating high surgical risk; patients assessed preoperatively by an evaluation team based on breast imaging to have partial breast defects, requiring combined flap repair or nipple-areola complex (NAC) reconstruction during surgery; patients with concurrent mental or psychological disorders; Patients with severe underlying medical conditions; Pregnant or breastfeeding women; Patients with significant thoracic deformities, such as pectus excavatum or pectus carinatum; Patients who refuse the procedure due to personal preference; Patients who have previously undergone breast reconstructive surgery (e.g., implant placement, ptosis correction, autologous fat transplantation, etc.). |
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研究实施时间: Study execute time: |
从 From 2025-07-01 00:00:00至 To 2026-07-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-08-01 00:00:00 至 To 2025-12-01 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: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
女性 |
Gender: |
Female |
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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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
无 |
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Blinding: |
None |
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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): |
None |
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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: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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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 |