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临床试验/NCT01336556
NCT01336556Unknown不适用

Optimal Titration of Continuous Positive Airway Pressure Could Predict Success of Oral Appliance to Treat Obstructive Sleep Apnea Syndrome

Associacao Fundo de Incentivo a Psicofarmcologia2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2010年10月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
2
主要终点
Objective sleep parameters

研究概览

简要总结

Background: The oral appliances have been increasingly used in the treatment of primary snoring and in patients with mild obstructive sleep apnea syndrome besides being treatment options in adults with moderate to severe sleep apnea who did not accept or adapt to continuous positive airway pressure (CPAP). It is not well established yet in the literature, which patients with mild to moderate OSA will present a good response to treatment with oral appliances.

Objective: To determine a value of CPAP pressure that correlates with a favorable response to the use of oral appliance in patients with mild to moderate sleep apnea.

Patients and Methods: Two groups of 30 male patients (25-65 years, body mass index < 35 kg/m2) will be selected: the first group with an apnea-hypopnea index (AHI) between 5 and 15 events per hour of sleep and the second one with an AHI between 15 and 30 events per hour of sleep. Each patient will undergo three polysomnographic recordings (baseline, CPAP titration, after two months of treatment with oral appliance). Subjective (sleep disorders questionnaire, the Epworth Sleepiness Scale, and sleep diaries) and objective (polysomnography) parameters of sleep will be evaluated, besides the quality of life (SF-36), mood (POMS), and anthropometric measurements (neck circumference and craniofacial characteristic). Good response to treatment with the AIO will be considered as a 50% reduction in the baseline AHI index or AHI after treatment less than 5 events per hour of sleep.

研究设计

研究类型
Interventional
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Male subjects aged between 25 and 65 years old
  • Epworth sleepiness Scale > 9
  • Apnea-hypopnea index between 5 and 30

排除标准

  • Presence of clinical disease (chronic obstructive pulmonary disease, asthma) and other sleep disorders.
  • Presence of anatomical obstructive upper airway, tonsil grade III e IV, septal deviation and grade III that may affect the outcome of CPAP
  • Loss of posterior dental support to undermine the retention of oral appliance
  • Active of periodontal disease, compared Dental crow/dental root less than or equal to 1 (c/r ≤ 1) need primary dental care (cavities, root canal treatment or retreatment, dentures, i.e. outlying), open bite
  • Protrusive displacement lass then five millimeters
  • Limited mouth opening
  • Alcoholism
  • Use of sleep-inducing medications
  • Habits or occupation that lead to sleep deprivation or alteration of the sleep-wake cycle
  • Intolerance to CPAP
  • Obesity grade II (moderate) or III (severe)

结局指标

主要结局

Objective sleep parameters

时间窗: two months after the baseline recording

polysomnographic date of sleep stages percentages, sleep efficience, arousals, apnea-hypopnea index, oxyhemoglobin saturation

次要结局

  • Subjective sleep parameters(two months after the baseline recording)
  • Quality of life, mood, and anthropometric measurements(two months after the baseline recording)

研究者

发起方
Associacao Fundo de Incentivo a Psicofarmcologia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. Lia Azeredo-Bittencourt

professor

Associacao Fundo de Incentivo a Psicofarmcologia

研究点 (2)

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