此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Laryngeal Mask Airway (LMA) Protector for Minimally Invasive Thyroidectomy

2017年11月12日 更新者:Georgios Kotsovolis、424 General Military Hospital

Study of the Laryngopharyngeal Symptoms After Minimally Invasive Thyroidectomy: Comparison Between the Protector Laryngeal Mask Airway and the Endotracheal Tube.

The patients will be allocated to 2 groups: the LMA group and the endotracheal tube (ET) group. Airway management will be done with the LMA Protector for the patients of the LMA group and with the classic endotracheal tube for the patients of the ET group. The main purpose of the study is to determine if the application of the LMA Protector causes less laryngopharyngeal symptoms than the endotracheal tube after minimally invasive thyroidectomy. The secondary purpose is to confirm that the LMA Protector is a safe alternative airway management device for minimally invasive thyroidectomy.

研究概览

研究类型

介入性

注册 (实际的)

79

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Thessaloniki、希腊、54636
        • Ahepa University Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 80年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Total thyroidectomy with the minimally invasive method.
  • American Society of Anesthesiologists (ASA) classification 1-3

Exclusion Criteria:

  • Clinical conditions which cause any kind of airway obstruction or compromise.
  • Tracheal displacement greater than 2cm from midline.
  • History of gastroesophageal reflux disease.
  • Expected difficult airway.
  • History of impossible intubation.
  • BMI>35
  • Reoperation within 24hours.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:LMA Protector
After induction of general anesthesia, the LMA Protector will be applied for airway management. The size of the laryngeal mask will be chosen according to the manufacturer's instructions. Lubricant gel will be applied to the dorsal side of the mask to ease the insertion to the oropharynx. The cuff of the mask will be filled with air by syringe until the indication of the integrated cuff pressure indicator is appropriate according to the manufacturer (green indication). If the indication changes during surgery, air will be added or removed accordingly. If the ventilation of the patient is inadequate at the beginning or anytime during the operation, the mask will be removed and the patient will be intubated
After induction of general anesthesia, the LMA Protector will be applied for airway management. The size of the laryngeal mask will be chosen according to the manufacturer's instructions. Lubricant gel will be applied to the dorsal side of the mask to ease the insertion to the oropharynx. The cuff of the mask will be filled with air by syringe until the indication of the integrated cuff pressure indicator is appropriate according to the manufacturer (green indication). If the indication changes during surgery, air will be added or removed accordingly. If the ventilation of the patient is inadequate at the beginning or anytime during the operation, the mask will be removed and the patient will be intubated.
有源比较器:Endotracheal tube
After induction of general anesthesia, the endotracheal tube be applied for airway management. The size of the tube will be 7.5 for female and 8.5 for male patients. The cuff of of the tube will be filled with 10ml air.
After induction of general anesthesia, the endotracheal tube be applied for airway management. The size of the tube will be 7.5 for female and 8.5 for male patients. The cuff of of the tube will be filled with 10ml air.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Postoperative sore throat.
大体时间:Within 20 minutes from the end of the procedure.
The patients will be asked to evaluate their postoperative constant pharyngeal pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
Within 20 minutes from the end of the procedure.
Postoperative sore throat.
大体时间:1 hour after the exit from the recovery room.
The patients will be asked to evaluate their postoperative constant pharyngeal pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
1 hour after the exit from the recovery room.
Postoperative sore throat.
大体时间:6 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative constant pharyngeal pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
6 hours after the exit from the recovery room.
Postoperative sore throat.
大体时间:12 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative constant pharyngeal pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
12 hours after the exit from the recovery room.
Postoperative sore throat.
大体时间:24 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative constant pharyngeal pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
24 hours after the exit from the recovery room.
Postoperative surgical site pain.
大体时间:Within 20 minutes from the end of the procedure.
The patients will be asked to evaluate their postoperative surgical trauma pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
Within 20 minutes from the end of the procedure.
Postoperative surgical site pain.
大体时间:1 hour after the exit from the recovery room.
The patients will be asked to evaluate their postoperative surgical trauma pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
1 hour after the exit from the recovery room.
Postoperative surgical site pain.
大体时间:6 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative surgical trauma pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
6 hours after the exit from the recovery room.
Postoperative surgical site pain.
大体时间:12 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative surgical trauma pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
12 hours after the exit from the recovery room.
Postoperative surgical site pain.
大体时间:24 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative surgical trauma pain by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
24 hours after the exit from the recovery room.
Postoperative dysphagia.
大体时间:Within 20 minutes from the end of the procedure.
The patients will be asked to evaluate their postoperative pharyngeal pain caused after swallowing one sip of water by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
Within 20 minutes from the end of the procedure.
Postoperative dysphagia.
大体时间:1 hour after the exit from the recovery room.
The patients will be asked to evaluate their postoperative pharyngeal pain caused after swallowing one sip of water by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
1 hour after the exit from the recovery room.
Postoperative dysphagia.
大体时间:6 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative pharyngeal pain caused after swallowing one sip of water by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
6 hours after the exit from the recovery room.
Postoperative dysphagia.
大体时间:12 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative pharyngeal pain caused after swallowing one sip of water by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
12 hours after the exit from the recovery room.
Postoperative dysphagia.
大体时间:24 hours after the exit from the recovery room.
The patients will be asked to evaluate their postoperative pharyngeal pain caused after swallowing one sip of water by using the 11grade Numerical Rating Scale (0 no pain, 10 maximum possible pain).
24 hours after the exit from the recovery room.

次要结果测量

结果测量
措施说明
大体时间
Airway management difficulty.
大体时间:3 minutes after induction of general anesthesia.
The efforts required to establish a secure airway and manage adequate patient ventilation will be recorded.
3 minutes after induction of general anesthesia.
Airway management complications.
大体时间:Within 5 minutes from induction of general anesthesia.
Any complication from airway management will be recorded like bleeding from the stomatopharynx or the larynx, tooth trauma, lip trauma, etc.
Within 5 minutes from induction of general anesthesia.
Emergence coughing.
大体时间:Within 10 minutes from the end of the surgery.
The incidence of cough upon emergence from general anesthesia will be recorded.
Within 10 minutes from the end of the surgery.
Postoperative paracetamol consumption.
大体时间:1, 6, 12 and 24 hours after emergence from general anesthesia.
The patients will be instructed to ask for analgesics as needed. When rescue analgesia is required 1000mg paracetamol will be administered. The frequency of paracetamol administration will be documented.
1, 6, 12 and 24 hours after emergence from general anesthesia.
Postoperative hoarseness.
大体时间:Within 20 minutes from the end of the procedure and after 1, 6, 12 and 24 hours.
The patients postoperative hoarseness will be evaluated according to the GRBAS scale.
Within 20 minutes from the end of the procedure and after 1, 6, 12 and 24 hours.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2017年2月1日

初级完成 (实际的)

2017年10月30日

研究完成 (实际的)

2017年11月1日

研究注册日期

首次提交

2017年3月22日

首先提交符合 QC 标准的

2017年3月28日

首次发布 (实际的)

2017年4月4日

研究记录更新

最后更新发布 (实际的)

2017年11月14日

上次提交的符合 QC 标准的更新

2017年11月12日

最后验证

2017年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • 184/15.03.2017

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

LMA Protector的临床试验

3
订阅