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临床试验/NCT03503656
NCT03503656已完成不适用

Evaluation and Usability of "Compuflo®" in Epidural Anesthesia for Obstetric and Gynecological Areas

Azienda Ospedaliero-Universitaria Careggi0 个研究点目标入组 140 人开始时间: 2017年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
140
主要终点
was the number of successes

研究概览

简要总结

Recently a computerized injection pump has been programmed with its own mathematical algorithm to measure on a digital display the pressure trend in the form of a continuous curve and it has been connected to an acoustic device that emits a sound at increasing frequencies during the progress of the epidural needle (Compuflo®, Milestone Scientific, Livingston, NJ); it has therefore been made capable of controlling the pressure at the injection point and adjusting the infusion rate according to a predetermined maximum value using the registered Dynamic Pressure Sensing (DPS) technology.

The Compuflo® system guarantees feedback on simultaneous and continuous pressure data, both visual and auditory, identifying and differentiating the different types of tissue. This safe and effective feedback helps medical personnel to identify the epidural space with greater accuracy and alerts them if the needle moves into the identified position.

The aim of the study was to verify the efficacy and usability of the Compuflo® system in a clinical setting.

The setting was the area of gynecology and obstetrics at a tertiary referral level University Hospital.

All the consecutive patients undergoing to an epidural catheter placement with Compuflo® were collected until to a sample size of 140 patients.

Primary endpoint was the number and percentage of successes in the placement of epidural catheters with Compuflo® Epidural. Secondary endpoints were: the number and percentage of accidental dural punctures during epidural catheter placement; the number of attempts aimed at the correct positioning of the epidural catheter; the measurement of procedure time duration; the measurement of pressure in the interspinous ligament, in the yellow ligament and within the epidural space; the measurement of volume of saline injected by Compuflo® to identify the epidural space.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

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

入选标准

  • signed informed consent to procedure more than 18 years of age

排除标准

  • 未提供

结局指标

主要结局

was the number of successes

时间窗: 18 months

number

次要结局

  • the number of attempts(18 months)
  • the number of accidental dural punctures(18 months)
  • procedure time duration(18 months)
  • measurement of volume of saline injected by Compuflo®(18 months)
  • measurement of pressure in the interspinous ligament, in the yellow ligament and within the epidural space(18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alessandro Di Filippo

Dr

Azienda Ospedaliero-Universitaria Careggi

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