|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2500115197 |
|
最近更新日期: Date of Last Refreshed on: |
2025-12-23 16:51:49 |
|
注册时间: Date of Registration: |
2025-12-23 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
阿波罗全适·乐蕊1.56网阵匀光镜片对青少年近视防控作用的研究 |
|
Public title: |
A Clinical trial to evaluate the impact of Apollo L.A.R.I Lenses on myopia prevention and control in adolescents |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
阿波罗全适·乐蕊1.56网阵匀光镜片对青少年近视防控作用的研究 |
|
Scientific title: |
A Clinical trial to evaluate the impact of Apollo L.A.R.I Lenses on myopia prevention and control in adolescents |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
陈晓琴 |
研究负责人: |
李丽华 |
|
Applicant: |
Chen Xiaoqin |
Study leader: |
Li Lihua |
|
申请注册联系人电话: Applicant telephone: |
+86 22 2721 7663 |
研究负责人电话:
Study leader's |
+86 22 2721 7663 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
chenxq017@163.com |
研究负责人电子邮件: Study leader's E-mail: |
tysgzxlccs@163.com |
|
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): |
||
|
申请注册联系人通讯地址: |
天津市和平区甘肃路4号 |
研究负责人通讯地址: |
天津市和平区甘肃路4号 |
|
Applicant address: |
No. 4, Gansu Road, Heping District, Tianjin City |
Study leader's address: |
No. 4, Gansu Road, Heping District, Tianjin City |
|
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: |
||
|
申请人所在单位: |
天津市眼科医院 |
||
|
Applicant's institution: |
Tianjin Eye Hospital |
||
|
研究负责人所在单位: |
天津市眼科医院 |
||
|
Affiliation of the Leader: |
Tianjin Eye Hospital |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
KY-2025044 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
天津市眼科医院医学伦理委员会 |
||
|
Name of the ethic committee: |
Medical Ethics Committees of Tianjin Eye Hospita |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-10-20 00:00:00 | ||
|
伦理委员会联系人: |
郭雅图 |
||
|
Contact Name of the ethic committee: |
Guo Yatu |
||
|
伦理委员会联系地址: |
天津市和平区甘肃路4号 |
||
|
Contact Address of the ethic committee: |
No. 4, Gansu Road, Heping District, Tianjin City |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 22 2731 3336 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
天津市眼科医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Tianjin Eye Hospital |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
天津市和平区甘肃路4号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 4, Gansu Road, Heping District, Tianjin City |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
由申办者广州市苏明达光学有限公司提供 |
||||||||||||||||||||||
|
Source(s) of funding: |
Provided by Sumingda Optics (Guang zhou) Co.,Ltd |
||||||||||||||||||||||
|
研究疾病: |
近视 |
||||||||||||||||||||||
|
Target disease: |
Myopia |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||
|
研究所处阶段: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
单臂 |
||||||||||||||||||||||
|
Study design: |
Single arm |
||||||||||||||||||||||
|
研究目的: |
评价阿波罗全适·乐蕊1.56网阵匀光镜片在近视进展控制中的有效性和安全性。 |
||||||||||||||||||||||
|
Objectives of Study: |
To evaluate the safety and efficacy of Apollo L.A.R.I Lenses in slowing myopia progression. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1)年龄6周岁≤年龄≤14周岁; 2)双眼主觉验光等效球镜(SE)-1.00D至-6.00D,散光≤1.00D,双眼近视度数参差≤1.00D; 3)双眼最佳矫正视力≥1.0; 4)受试者及其法定监护人必须签署知情同意书,愿意配合治疗及随访,并自愿参加本研究。 |
||||||||||||||||||||||
|
Inclusion criteria |
1. Age >=6 years old and <=14 years old,; 2. The equivalent spherical diopter of objective refraction is between>= -1.00 D and <= -6.00 D, with astigmatism <= 1.00D and refractive error of both eyes <= 1.00D after the equivalent spherical diopter; 3. The best corrected visual acuity in both eyes is >=1.0; 4. Voluntarily participate in this clinical trial and sign the informed consent form. |
||||||||||||||||||||||
|
排除标准: |
1)单眼符合入选标准; 2)双眼显性斜视或存在明显视功能异常; 3)存在影响眼部的全身性疾病; 4)确诊病理性近视及其它先天性眼病; 5)不愿配合访视者; 6)研究者判断患者不适合入选的其它情况。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1.Only one eye meets the inclusion criteria; 2.Binocular dominant strabismus or obvious visual function abnormalities; 3.There are systemic diseases that affect the eyes; 4.Diagnosis of pathological myopia and other congenital ocular disorders; 5.Those who fail to follow up regularly as required by the test; 6.The researchers determined that the candidates could not be selected. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2025-12-25 00:00:00至 To 2026-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-12-30 00:00:00 至 To 2026-03-01 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
|
盲法: |
无 |
|
Blinding: |
None |
|
是否共享原始数据: IPD sharing |
否No |
|
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 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
N/A |
|
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: |
电子采集和管理 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |