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临床试验/NCT02428413
NCT02428413已完成不适用

Evaluation and Control of Waste Anesthetic Gas (WAG) in the Post Anesthesia Care Unit (PACU) Within Patient and Caregiver Breathing Zone

Teleflex0 个研究点目标入组 125 人开始时间: 2015年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Teleflex
入组人数
125
主要终点
Waste Anesthetic Gas Measured by Parts Per Million Emanating From Patients During Normal PACU Working Conditions

研究概览

简要总结

The purpose of this study is to evaluate anesthetic gas in the PACU within patient and caregiver breathing zones.

详细描述

The purpose of this single-center, multi-arm, randomized controlled study is to evaluate use of the ISO-Gard mask in patients immediately following a surgical procedure in which inhaled anesthetic is used as the primary modality of anesthesia, for the following: 1) measure the waste anesthetic gas emanating from patient during the immediate one hour post-operative recovery period in the PACU; 2) measure waste anesthetic gas within PACU caregiver's breathing zone; and 3) determine the efficacy of the ISO-Gard mask in reducing caregiver's exposure to waste anesthetic gas in the PACU.

Subjects who will receive either Sevoflurane or Desflurane inhaled anesthetic will be enrolled in this study. Subjects will be randomized to receive either the ISO-Gard scavenging mask or a traditional supplemental oxygen mask post operatively; all other elements of the subjects' care will be in accordance with the institution's standard of care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Subject is 18-120 years of age.
  • Patients requiring inhaled anesthetic agents as part of their anesthesia during surgery (Sevoflurane or Desflurane)
  • Patients with following outpatient procedures scheduled for a duration of greater than 2 hours per the operating room schedule:
  • . Bariatric procedures
  • Robotic surgery cases
  • Gynecological procedures
  • Not documented as terminally ill
  • Subject expected to remain in PACU for at least one hour
  • Subject or legally authorized representative has provided written informed consent prior to the procedure using a form that is approved by the Institutional Review Board (IRB).

排除标准

  • Patients are/were given/planned to be given total IV anesthetics during surgery
  • Any patient that is not expected to tolerate a mask in PACU
  • Subject has already been enrolled in study
  • Subject is an employee of the Investigator or has involvement in other studies under the direction of investigator or study site
  • Women who are pregnant
  • End of anesthetic gas administration in PACU bay greater than 45 minutes

结局指标

主要结局

Waste Anesthetic Gas Measured by Parts Per Million Emanating From Patients During Normal PACU Working Conditions

时间窗: 1 hour post-operative recovery period

The measurement of Waste Anesthetic Gas in parts per million emanating from the patient between the standard oxygen mask and the ISO-Gard oxygen mask.

Efficacy of the ISO-Gard Mask in Reducing Caregiver's Exposure to WAG-Duration

时间窗: 1 hour post-operative recovery period

For MAX-WAG measurements obtained every 30 seconds, we calculated the duration of MAX-WAG \[\>2ppm\]

Waste Anesthetic Gas Measured by Parts Per Million Within PACU Caregiver's Breathing Zone With Caring for Patients

时间窗: 1 hour post-operative recovery period

The measurement of Waste Anesthetic Gas in parts per million resolution emanating from the patient to the caregiver's breathing zone.

Efficacy of the ISO-Gard Mask in Reducing Caregiver's Exposure to WAG-Percentage of Time

时间窗: 1 hour post-operative recovery period

For MAX-WAG measurements obtained every 30 seconds, we calculated the percentage of time in MAX-WAG \[\>2ppm\] relative to the total collection period.

次要结局

未报告次要终点

研究者

发起方
Teleflex
申办方类型
Industry
责任方
Sponsor

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