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美国临床详情页--结果指标

websocket测试

POST

/libraries/american/getUsClinicalDetailTracking

请求参数

参数名

类型

描述

必填

clinical_id

string

临床试验id

必填

响应参数

参数名

类型

描述

必填

code

int

示例：200

必填

msg

string

示例：查询成功

必填

data

array

数据列表

必填

first_submitted

string

首次提交日期

必填

first_posted

string

首次发布日期

必填

last_update_posted

string

最后更新发布日期

必填

estimated_start

string

预计研究开始日期

必填

current_primary_measures

array

目前的主要结果指标，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

original_primary_measures

array

原始的主要结果指标，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

change_history

array

变更记录，以{"titile":"变更记录标题","href":"变更链接"}格式标识

必填

current_secondary_measures

array

目前的次要结果指标，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

original_secondary_measures

array

原始的次要结果指标，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

current_other_measures

array

当前其他预先指定的成果措施，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

original_other_measures

array

其他原先预定的成果措施，以{"段落1","段落2",}格式保存段落信息，注意保留缩进

必填

说明 / 示例

{ "code": 200, "msg": "查询成功", "data": [ { "first_posted": "2010-03-16", "last_update_posted": "2020-12-19", "estimated_start": "2010-02-18", "current_primary_measures": [ "Analyze GSMS results for rare disorders for which genetic causes are known but not fully described [ Time Frame: Ongoing ]We aim to sequence penetrant cases to study the molecular variations of rare genetic disorders, to better predict pathogenicity and identify new causative variants.", "Molecular etiology of rare diseases [ Time Frame: Ongoing ]Identify the genetic cause of disorders that are intractable or difficult to identify with existing techniques, for example, disorders due tonew mutations with poor reproductive fitness though whole exome or whole genome sequencing" ], "original_primary_measures": null, "change_history": null, "current_secondary_measures": null, "original_secondary_measures": null, "current_other_measures": null, "original_other_measures": null } ] }

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