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临床试验/NL-OMON53268
NL-OMON53268招募中不适用

Methodological trial to investigate the dose-response relationship, test-retest reliability and tolerance to repeated exposure of the 35% carbon dioxide experimental panic challenge in CO2-sensitive healthy volunteers - Methodological optimization of the CO2 challenge

Centre for Human Drug Research0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational invasive

入排标准

年龄范围
18 至 64(—)

入选标准

  • 1. Healthy male or female aged between 18 and 65 years (inclusive) at screening
  • who have been demonstrated to be sensitive to the panicogenic effects of the
  • CO2 challenge in previous studies;
  • 2. Sensitivity to the fear-inducing effects of 35% CO2 double-breath inhalation
  • is defined as an increase from pre-CO2 to post-CO2 challenge in the following:
  • PSL-IV total scores >=4 with at least 1-point increase for at least 4 of the
  • symptoms specified in the PSL-IV and an increase on the Visual Analog Scale
  • (VAS) Fear of at least 25 mm;
  • 3. BMI of 18-32 kg/m2 (inclusive);
  • 4. Non-smoker for at least 3 months.

排除标准

  • 1. Subjects with a clinically significant current or past personal or family
  • history of any psychiatric disorder as classified by DSM-4 or DSM-5 criteria.
  • 2. Current or past history of alcohol or any substance abuse or dependence
  • disorder within the past 12 months;
  • 3. Clinically significant ECG abnormalities;
  • 4. Clinically significant abnormality of the lungs (e.g. COPD, asthma, lung
  • fibrosis) and hematologic diseases concerning hemoglobin (e.g. thalassemia and
  • sickle cell disease);
  • 5. Important cardiovascular history, or suspicion of infarct, cardiomyopathy,
  • cardiac failure, TIA, angina pectoris, cardiac arrhythmias, CVA;
  • 6. Personal or familial history of cerebral aneurysm.

研究者

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