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【ChiCTR-IOR-15007421】以 "外科癒合劑" 或 "縫針" 方法處理傷口之成效研究計劃

基本信息
登记号

ChiCTR-IOR-15007421

试验状态

尚未开始

药物名称

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药物类型

/

规范名称

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首次公示信息日的期

2015-11-18

临床申请受理号

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靶点

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适应症

lacerated wound

试验通俗题目

以 "外科癒合劑" 或 "縫針" 方法處理傷口之成效研究計劃

试验专业题目

以 "外科癒合劑" 或 "縫針" 方法處理傷口之成效研究計劃

申办单位信息
申请人联系人
申请人名称
联系人邮箱
联系人邮编

联系人通讯地址
临床试验信息
试验目的

以 "外科癒合劑" 或 "縫針" 方法處理傷口之成效

试验分类
试验类型

随机平行对照

试验分期

其它

随机化

Parallel 1:1 ratio by using computer generated method with block size four.

盲法

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试验项目经费来源

Nethersole school of Nursing

试验范围

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目标入组人数

0;15

实际入组人数

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第一例入组时间

1990-01-01

试验终止时间

1990-01-01

是否属于一致性

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入选标准

The inclusion criteria are listed as follows: (a) Chinese pediatric patients, 7 years to 17 years; (b) with sustained laceration wound of <5 cm in length but without deep structure injury (bone and joint involvement or neurovascular damage to the tissue being repaired); and 3) availability of parent consent.;

排除标准

The exclusion criteria are listed as follows: (a) underlying structural injury (e.g., muscle, tendon, bone, joint, or neuro-muscular injury, and scalp wounds); (b) complicated wound (severely crushed injury or stellate lacerations in areas with dense natural hair or under prolonged moisture or friction); (c) injury in mucosal surfaces, across muco-cutaneous junctions (e.g., oral cavity and lips), or skin, which may be regularly exposed to bodily fluids; d) high risk of infection (heavily contaminated, actively infected wounds, animal bites, or wounds sustained for more than 12 hours, and wound requiring debridement to remove nonviable tissue); e) high tension (e.g., chin) or deep wound that required deep sutures (e.g., torso or joint); f) eyelid or peri-orbital laceration; g) known hypersensitivity to tissue adhesive; and h) psychiatric cognitive disorder indicated in medical record (such as autism and mental retardation); h) wound that have potentially important consequences as perceived by parents.;

研究者信息
研究负责人姓名
试验机构

Eliza Wong

研究负责人电话
研究负责人邮箱
研究负责人邮编

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联系人通讯地址
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