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临床试验/NCT02505763
NCT02505763Unknown不适用

Treatment of Pleural Effusion by Routine Thoracic Ultrasound

University Hospital, Toulouse2 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2017年7月10日最近更新:
适应症

试验速览

阶段
不适用
入组人数
144
试验地点
2
主要终点
The cost-effectiveness ration

研究概览

简要总结

The main objective of the study is to assess the cost-effectiveness ratio of two management strategies of pleurisy in adults : a strategy by systematic thoracic ultrasound versus a strategy without thoracic ultrasound.

详细描述

Comparison of two management strategies pleural effusions from diagnosis and during the first year of follow up care.

Patients are randomized into two groups, each group receiving a different management strategy.

Both strategies are compared:

Strategy A that involves the systematic use of thoracic ultrasound for the treatment of pleural effusion, treatment and follow up care. It will be possible to have recourse to other tests (such as chest CT) if deemed necessary by the practitioner.

Strategy B, which consists of the usual care pleurisy and thus without use of ultrasound: gestures are guided either by chest radiograph or by CT chest as necessary in the treatment and monitoring. A systematic radiographic pleural after each gesture is performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients hospitalized or seen in consultation with pleural effusion diagnosed clinically or radiologically whatever be its initial management.

排除标准

  • Patient with a neoplasia

结局指标

主要结局

The cost-effectiveness ration

时间窗: 1 year

Cost estimates will be conducted from the perspective of health insurance. The expenses incurred in the care of patients with pleurisy will be counted in both groups during the follow-up year. The effectiveness will be assessed against the complications of strategy (pneumothorax, respiratory sequelae, surgery, mortality, chest pain sequelae, radiological consequences).

次要结局

  • The duration of hospitalization(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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