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临床试验/TCTR20210218005
TCTR20210218005招募中3 期

Efficacy of Armodafinil in Moderate to Severe Obstructive Sleep Apnea Patients with Residual Excessive Daytime Sleepinesss after Suboptimal Usage of Continuous Positive Airway Pressure Treatment: A Prospective Cohort Study

Ratchadapiseksompoj funds0 个研究点目标入组 30 人开始时间: 2021年2月18日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Patient who diagnosed with moderate to severe OSA and still have excessive daytime sleepiness defined as ESS >10 and have received stable CPAP therapy at least 4 weeks but in suboptimal usage
  • patient naive to Armodafinil

排除标准

  • 1.Patient who was diagnosed with sleep disorders other than OSA
  • 2.Patient who has clinically significant or uncontrolled medical condition, treated and untreated, or any disorder that might interfere with drug absorption, distribution, metabolism, excretion or produce daytime sleepiness
  • 3.Patient use prescription drugs disallowed by protocol* or clinically significant use of over-the-counter drugs within 7 days before baseline visit
  • 4.Patient with history of alcohol, narcotics, or any other recreational drug abuse
  • 5.Patient with excessive consumption of caffeine > 600 mg/day or > 8 cups/day
  • 6.Patient who is pregnancy or lactation
  • 7.Patients with psychiatric disorders
  • 8.Patients with cardiovascular disorder
  • - History of Left Ventricular Hypertrophy (LVH)
  • - Mitral Valve Prolapse (MVP) who have experienced MVP syndrome with previous CNS stimulant exposure
  • - Unstable Cardiovascular (CV) disease
  • - Moderate to severe symptomatic Cardiovasbular (CV) disease
  • 9.Patients with abnormal ECG at baseline or uncontrolled blood pressure ( >180/100 mmHg)

研究者

发起方
Ratchadapiseksompoj funds

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