跳至主要内容
临床试验/NL-OMON50574
NL-OMON50574已完成不适用

Functional Neural Correlates of Transcutaneous Vagal Nerve Stimulation: Effects of Anatomical Site and Waveform Parameters * An exploratory High Resolution fMRI Study in Healthy Volunteers - Neural collerates of tVNS

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • * Of female sex;
  • * Healthy participants (defined as those without a pre-existing medical
  • comorbidity)
  • * Age between 18 and 40 years;
  • * BMI between 18 and 30 kg/m2;
  • * All subjects should be on oral contraceptives
  • * All subjects should be right-handed.
  • * Inclusion will be determined on the basis of availability. They should be
  • able to attend for 2 scanning sessions.

排除标准

  • * Presence of metallic prostheses, pacemakers, metal clips on blood vessels,
  • metal parts in the eye, an intrauterine device, metal braces, tattoos and/or
  • other metal objects;
  • * History of major head trauma or head/brain surgery;
  • * History of claustrophobia;
  • * History of severe or chronic cardiovascular, respiratory, urogenital,
  • gastrointestinal/ hepatic, hematological/immunologic, HEENT (head, ears, eyes,
  • nose, throat), dermatological/connective tissue, musculoskeletal,
  • metabolic/nutritional, endocrine, neurological/psychiatric diseases, major
  • surgery and/or laboratory assessments which might limit participation in or
  • completion of the study protocol;
  • * Use of regular medication, including vitamin and iron supplementation, except
  • oral contraceptives, within 14 days prior to start of the study;
  • * Pregnancy, lactation, wish to become pregnant;
  • * High alcohol consumption (>15 alcoholic units consumed per week);
  • * Using drugs of abuse;
  • * Administration of investigational drugs or participation in any scientific
  • intervention study which may interfere with this study (to be decided by the
  • principle investigator), in the 180 days prior to the study;
  • * Any evidence of structural brain abnormalities examined by anatomical MRI
  • will lead to exclusion
  • * Participants unable to provide informed consent
  • * Participants with any systemic disease or medications that may influence the
  • autonomic nervous system (e.g. beta-agonists or Parkinson*s disease)
  • * Current smokers or current use of nicotine in any other way (including
  • E-cigarettes and patches)
  • * History of clinical anxiety or depression, or a hospital anxiety or
  • depression score >8
  • * Patient whom have cardiovascular conduction problems
  • * Patient with cochlear implants
  • * Not meeting any of the inclusion criteria above
  • * Participants whom score 8 or more on the HADS-questionnaire at study
  • commencement

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

相似试验