跳至主要内容
临床试验/NCT02605928
NCT02605928已完成不适用

INJ-INAR-01 Use of BIP-Needles in Rheumatologic Injections

Injeq Ltd1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2014年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
1
主要终点
True Positive Detection of Synovial Fluid Marked in Case Report Form

研究概览

简要总结

The study focuses on needle guidance in rheumatologic operations - glucocorticoid injections inside joint capsules specifically. The main purpose of the study is to assess and validate the clinical feasibility and performance of Bioimpedance Probe (BIP) Needles and assess the benefits, drawbacks and risks related to use of the BIP Needles.

详细描述

Clinical device investigation

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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
是

入选标准

  • •Adult patients having an inflammatory rheumatic disease requiring an intra-articular glucocorticoid injection.

排除标准

  • •Exclusion criteria are the same as generally for intra-articular glucocorticoid injections (e.g. bacterial infection or recent surgical operation relating the joint).
  • •In addition for not giving (or not capable to give) the consent personally for any reason is an absolute exclusion criterion.
  • •In addition pregnant women are excluded

研究组 & 干预措施

BIP Needle

Experimental

Injeq Bioimpedance Probe (BIP) Needle is an injection needle that has bioimpedance measurement capability. It measures bioimpedance and detects synovial fluid during inta-articular injection.

干预措施: Injeq Bioimpedance Probe (BIP) Needle (Device)

结局指标

主要结局

True Positive Detection of Synovial Fluid Marked in Case Report Form

时间窗: During intra-articular injection

Measurement device indicates with a sound and visual feedback when needle is in contact with synovial fluid. Physician verifies the location with ultrasound imaging, aspiration of synovial fluid and/or lack of resistance in glucocorticoid injection. Even if the device does not detect the synovial fluid, physician performs the injection when needed. Physician marks to the case report form whether the device provided detections during the puncture and were the detections true or false detections.

次要结局

未报告次要终点

研究者

发起方
Injeq Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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