ChiCTR2200062196 版本V1.0 版本创建时间2022/07/29 10:03:29 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2200062196 

最近更新日期:

Date of Last Refreshed on:

2022-07-29 10:03:21 

注册时间:

Date of Registration:

2022-07-29 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

子宫腺肌病病灶切除手术术中缝合固定左炔诺孕酮宫内缓释系统:一种治疗难治性腺肌病的新手术方法

Public title:

Laparotomy combined with levonorgestrel-releasing intrauterine system: A new surgical method for refractory adenomyosis treatment

注册题目简写:

English Acronym:

研究课题的正式科学名称:

子宫腺肌病病灶切除手术术中缝合固定左炔诺孕酮宫内缓释系统:一项前瞻性临床研究

Scientific title:

Laparotomy combined with levonorgestrel-releasing intrauterine system: A prospective clinical study

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:

李瑜 

研究负责人:

李瑜 

Applicant:

YU LI 

Study leader:

YU LI 

申请注册联系人电话:

Applicant telephone:

+8618049920519

研究负责人电话:

Study leader's
telephone:

+8618049920519

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:

liyu19831221@126.com

研究负责人电子邮件:

Study leader's E-mail:

liyu19831221@126.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:

中国上海浦东新区高科西路2699号

研究负责人通讯地址:

中国上海浦东新区高科西路2699号

Applicant address:

No. 2699 Gaoke west Road, Pudong district, Shanghai, China

Study leader's address:

No. 2699 Gaoke west Road, Pudong district, Shanghai, China

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:

同济大学附属第一妇婴保健院

Applicant's institution:

Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

研究负责人所在单位:

同济大学附属第一妇婴保健院

Affiliation of the Leader:

Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

KS22229

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:

上海市第一妇婴保健院伦理委员会

Name of the ethic committee:

Ethics Committee, Shanghai First Maternity and Infant Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2022-06-10 00:00:00

伦理委员会联系人:

罗烨

Contact Name of the ethic committee:

YE LUO

伦理委员会联系地址:

中国上海浦东新区高科西路2699号

Contact Address of the ethic committee:

No. 2699 Gaoke west Road, Pudong district, Shanghai, China

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:

研究实施负责(组长)单位:

同济大学附属第一妇婴保健院

Primary sponsor:

Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

研究实施负责(组长)单位地址:

中国上海浦东新区高科西路2699号

Primary sponsor's address:

No. 2699 Gaoke west Road, Pudong district, Shanghai, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海

市(区县):

浦东新区

Country:

China

Province:

Shanghai

City:

shanghai

单位(医院):

同济大学附属第一妇婴保健院

具体地址:

中国上海浦东新区高科西路2699号

Institution
hospital:

Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

Address:

2699 Gaoke west Road, Pudong district, Shanghai, China

经费或物资来源:

政府拨款

Source(s) of funding:

Government appropriations

研究疾病:

子宫腺肌症  

Target disease:

adenomyosis

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

本课题拟开展一项前瞻性观察性临床研究,纳入约50名弥漫性难治型子宫腺肌病患者,采用改良版手术方法——切除子宫腺肌病病灶同时缝合固定LNG-IUS(商品名“曼月乐”)于宫腔内,比较手术前后月经量、痛经程度、血CA125值及子宫体积等变化,来验证该方案的有效性和可靠性。此研究以期通过长时间固定LNG-IUS来达到持续的治疗效果,为弥漫性难治型子宫腺肌病患者找到有效安全的保留子宫的手术方式,并为后续研究和临床运用的推广提供可行性建议及治疗依据。  

Objectives of Study:

In this project, a prospective observational clinical study is proposed, including about 50 patients with diffuse refractory adenomyosis, using an improved surgical method - excision of adenomyosis lesions and suturing and fixing LNG-IUS (trade name "Mirena") in the uterine cavity, comparing changes in menstrual volume, degree of dysmenorrhea, blood CA125 value and uterine volume before and after surgery to verify the effectiveness and reliability of the protocol. This study aims to achieve sustained therapeutic effect by fixing LNG-IUS for a long time, find an effective and safe surgical method for patients with diffuse refractory adenomyosis, and provide feasibility recommendations and treatment basis for follow-up research and clinical application.

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经过B超或MRI诊断为弥漫性子宫腺肌病或大病灶腺肌病,病灶直径大于5 cm,宫腔深度大于10 cm,并确认子宫腺肌病病灶深达内膜;②曾经应用单纯性药物治疗但效果不佳;或者曾经有腹腔镜切除子宫腺肌病病灶的经历,但治疗效果不理想;③年龄范围在20-45岁,并且2年内无生育要求;④充分知情且同意入组的患者。

Inclusion criteria

① Patients diagnosed with diffuse or giant adenomyosis using B-scan ultrasound or MRI, where the lesion diameter exceeded 5 cm, depth of the uterine cavity was greater than 10 cm and the depth of the lesion was confirmed to reach the endometrium; ② Patients who had previously received drug therapy or laparoscopic lesion resection, but the results were unsatisfactory; ③ Women in the age group of 20–45 years, who had no fertility requirements within the last 2 years.

排除标准:

①同时合并妇科其它器官的疾病,比如子宫颈病变、卵巢肿瘤等;②合并妇科阴道炎症等放置节育环的相关禁忌症;③有孕激素治疗的相关禁忌症;④有其它内外科基础疾病而无法行手术治疗的情况;⑤不同意入组的患者。

Exclusion criteria:

① Patients diagnosed with gynecological diseases other than adenomyosis, such as cervical lesions and ovarian tumors, as well as those with vaginal inflammation and other contraindications to intrauterine device (IUD) placement; ② Patients with contraindications to progesterone therapy; ③ Patients diagnosed with other gynecological conditions that cannot be treated with surgery.

研究实施时间:

Study execute time:

From 2022-07-28 00:00:00 To 2023-07-28 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-07-28 00:00:00 To 2023-07-28 00:00:00

干预措施:

Interventions:

组别:

连续入组

样本量:

50

Group:

consecutive

Sample size:

干预措施:

干预措施代码:

Intervention:

none

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

同济大学附属第一妇婴保健院 

单位级别:

三级甲等 

Institution
hospital:

Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

CA 125

指标类型:

主要指标

Outcome:

CA 125

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

CA 19-9

指标类型:

主要指标

Outcome:

CA 19-9

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

月经量评分

指标类型:

主要指标

Outcome:

Pictorial Blood Loss Assessment Chart

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

疼痛评分

指标类型:

主要指标

Outcome:

Visual Analogue Scale

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

子宫体积

指标类型:

主要指标

Outcome:

Uterine size

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

血液

组织:

Sample Name:

blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 20 years
最大 Max age 45 years

性别:

女性

Gender:

Female

随机方法(请说明由何人用什么方法产生随机序列):

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:

Blinding:

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):

no

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

no

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:

病历记录表

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-07-29 10:03:22