跳至主要内容
临床试验/NCT06403852
NCT06403852已完成2 期

Investigating Near-Threshold Perception During Anesthetic Sedation

University of Michigan2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年5月10日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
36
试验地点
2
主要终点
Blood Oxygen Level Dependent (BOLD) response to visual stimuli

研究概览

简要总结

The researchers expect to gain a deeper understanding of mental function during different levels of anesthesia, and to evaluate if the use of ultrasonic brain stimulation accelerates return to consciousness.

Propofol is FDA approved for use in patients undergoing an anesthetic for medical treatment but is not approved for use in healthy volunteers.

详细描述

The stimulus set will include real and scrambled images, where the scrambled images will be created by phase-shuffling a randomly chosen real image from each category to preserve category specific low-level image features. Because scrambled images do not include an object stimulus, the images are used as "catch trials" to determine the subjects' baseline tendency to give positive responses to a question about the subjects' recognition experience. Each object category will include four unique real images and one scrambled image. Each image will be repeated 10 times (i.e., trials) for each 16-min session. The pre-stimulus interval will vary randomly from trial to trial between 4 and 8 seconds to prevent stimulus timing predictability. The stimuli will be presented in a randomized order to prevent category predictability.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy study subjects with American Society of Anesthesiologists (ASA)-1 status.
  • Right-handed
  • Body mass index (BMI) less than
  • All subjects will be English speakers.

排除标准

  • Medical contraindication to magnetic resonance imaging (MRI) scanning; are unable to undergo MRI scanning because of possible pregnancy or currently breastfeeding, BMI>30, metallic substances in the body, claustrophobia, anxiety, or cardiopulmonary disease; or have an intracranial structural abnormality on T1-weighted MRI scans.
  • History of allergy to propofol, eggs or egg products, soybean or soybean products, neurological, cardiovascular, or pulmonary illness; significant head injury with loss of consciousness; learning disability or other developmental disorder; sleep apnea or any severe snoring history; gastroesophageal reflux disease (GERD) or heartburn; pancreatitis or a history of pancreatitis, or sensory/motor loss sufficient to interfere with performance of the study.
  • Tattoos in the head or neck region will be excluded from study; other tattoos are subject to determination by investigators based on their assessment regarding participant safety. To eliminate aspiration risk subjects will also be excluded if they have had recent food or liquid intake (within 8 hours).
  • History of drug use, have a positive drug screen, are unwilling to abstain from alcohol for 24 hours prior to dosing, or have a current history of nicotine use.
  • Pregnancy

结局指标

主要结局

Blood Oxygen Level Dependent (BOLD) response to visual stimuli

时间窗: Up to 90 minutes

Visual stimuli evoked activity was quantified by measurements of the fMRI BOLD signal. Neural response to a natural visual stimulus will be assessed during both conscious and anesthetized states.

次要结局

  • Perceptual criterion (c) derived from the Signal Detection Theory (SDT)(Up to 90 minutes)
  • Sensitivity (d') criterion derived from the Signal Detection Theory (SDT)(Up to 90 minutes)

研究者

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

Zirui Huang

Research Assistant Professor, Anesthesiology and Research Fellow

University of Michigan

研究点 (2)

Loading locations...

相似试验