Evaluation of Atomoxetine and Oxybutynin for Obstructive Sleep Apnea in Children With Down Syndrome
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 22
- 试验地点
- 1
- 主要终点
- Obstructive Apnea-hypopnea Index (oAHI)
研究概览
简要总结
This is a randomized, double blind, cross-over study of the combination of atomoxetine and oxybutynin (ato-oxy) in children with DS and OSA documented by polysomnography (PSG). Participants will receive high dose ato-oxy for four weeks as well as low dose ato-oxy for four weeks in random order. During the high dose ato-oxy period, participants will take 5 mg oxybutynin and 0.5mg/kg/day (max 40 mg) atomoxetine nightly for one week. Atomoxetine dose will then be increased to 1.2 mg/kg/day (max 80 mg). During the low dose ato-oxy period, participants will take 5 mg oxybutynin and 0.5mg/kg/day (max 40 mg) atomoxetine. Dosing of the study treatment will occur approximately 30 minutes prior to bedtime. Participants who withdraw from the study will not be replaced.
Study participants will undergo eligibility screening that will include an initial screening to determine whether non- PSG enrollment criteria are met, followed by a 1 night in-lab PSG and health-related quality of life assessment for participants who qualify based on non-PSG criteria. For participants who are eligible and enroll in the study, the screening PSG night will serve as the baseline measure for apnea hypopnea index (AHI) and other PSG endpoints. On the final night of dosing for both high dose ato-oxy and low-dose ato-oxy, participants will return for inpatient PSG and health-related quality of life assessment. The primary efficacy endpoint is the change in obstructive AHI from baseline (high dose ato-oxy vs. low dose ato-oxy).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 6 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female participants between 6 to 17 years of age, inclusive, at the Screening Visit. Enrollment will be stratified to ensure equal representation of children age 6-12 and age 13-
- •No more than 14 subjects will be randomized for each age group.
- •Known diagnosis of Down syndrome (trisomy 21, but not translocation or mosaicism)
排除标准
- •Hypoxemia independent of respiratory events on polysomnography (≥5 minutes with oxygen saturation <90%)
- •Presence of central sleep apnea on polysomnography (central AHI ≥ 5)
- •Currently using and adherent to PAP therapy (>4 hours per night for 70% of nights in the past 30 days based on device download or parent report)
- •MAO inhibitor use
- •Urinary retention
- •Prematurity < 37 weeks estimated gestational age
- •Seizure disorder
- •Untreated or inadequately treated hypothyroidism
- •Significant traumatic brain injury
- •Congenital heart disease and not cleared to participate by the patient's cardiologist
- •History of current, untreated depression
- •History of liver disease
- •3+ or greater tonsillar hypertrophy.
研究组 & 干预措施
High dose ato-oxy
干预措施: Atomoxetine and oxybutynin (ato-oxy) (Drug)
Low dose ato-oxy
干预措施: Atomoxetine and oxybutynin (ato-oxy) (Drug)
结局指标
主要结局
Obstructive Apnea-hypopnea Index (oAHI)
时间窗: four weeks
change in number of obstructive apneas and hypopneas per hour on polysomnography from baseline
次要结局
- Arousal Index(four weeks)
- Obstructive Sleep Apnea-18 Score (OSA-18)(four weeks)
研究者
Daniel A. Combs
Assistant Professor of Pediatrics
University of Arizona