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Supplemental Oxygen for Sleep-Disordered Breathing in Adults With Chronic Opioid Use. (OPIO2)

2026年11月2日 更新者:Jeremy Orr, M.D.、University of California, San Diego

Opioid Physiology and Individual Outcomes With Supplemental O₂ (OPIO2)

This study will evaluate whether supplemental oxygen given during sleep improves breathing stability and sleep-disordered breathing in adults who use prescription opioids long term.

Participants will receive both supplemental oxygen and sham air during separate overnight sleep studies in a randomized order. The two study conditions will be separated by a washout period of approximately one week. Researchers will compare breathing during sleep with supplemental oxygen versus sham air and will also evaluate measures of oxygen levels, carbon dioxide levels, sleep quality, alertness, and other aspects of breathing and sleep.

For participants who previously took part in the GENESIS study, qualifying assessments from that study may be used to meet certain baseline requirements when appropriate, which may reduce the need to repeat some testing.

研究概览

详细说明

This is a Phase II, single-center, randomized, double-blind, sham-controlled crossover study evaluating the effects of nocturnal supplemental oxygen on ventilatory stability and sleep-disordered breathing in adults receiving chronic opioid therapy.

Eligible participants will be randomized to one of two treatment sequences: supplemental oxygen followed by sham air, or sham air followed by supplemental oxygen. Each intervention will be administered during a separate in-laboratory overnight polysomnography (PSG) visit, with an approximately 1-week washout period between intervention nights. Each participant will therefore receive both study conditions and serve as their own control.

The study will evaluate the effect of supplemental oxygen on flow-based apnea-hypopnea index (AHIflow) and other measures of respiratory physiology, sleep-disordered breathing, oxygenation, carbon dioxide levels, neurobehavioral performance, and patient-reported sleep outcomes.

Most participants are expected to have previously enrolled in the GENESIS study (IRB #814091). When appropriate, qualifying assessments previously completed through GENESIS may be used to satisfy corresponding OPIO2 baseline requirements. OPIO2 informed consent, confirmation of current eligibility, and any required missing or repeat assessments must be completed before randomization.

研究类型

介入性

注册 (估计的)

62

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • California
      • La Jolla、California、美国、92037
        • Altman Clinical and Translational Research Institute
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 75年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age 18 to 75 years.
  • Chronic opioid use for ≥3 months with a daily opioid dose equivalent to at least 20 mg of oral morphine (morphine equivalent daily dose [MEqD]). Examples include approximately 13 mg oxycodone, 20 mg hydrocodone, 100 mg tramadol, or equivalent doses of other opioids.
  • Ability and willingness to comply with study procedures, including overnight laboratory polysomnography and administration of oxygen or sham air in the laboratory.
  • Ability to provide written informed consent.
  • For participants able to become pregnant: agreement to use an effective contraceptive method (e.g., a licensed hormonal or intrauterine method, or an effective barrier method) during study participation. The study team will review and document the method before enrollment.
  • Recruitment will target approximately equal numbers of males and females to enable consideration of sex as a biological variable, consistent with NIH policy.

In addition to the enrollment criteria, participants must meet the following criterion to be eligible for randomization:

• Diagnosis of sleep-disordered breathing (SDB), defined as AASM-recommended apnea-hypopnea index (AHI3A) ≥5 events per hour on a qualifying sleep study. AHI3A includes hypopnea definition ≥30% airflow reduction lasting ≥10 seconds, accompanied by ≥3% SpO2 desaturation or arousal.

Exclusion Criteria:

  • Body mass index (BMI) >35 kg/m².
  • Requirement for supplemental oxygen therapy outside of the study.
  • Current use of CPAP or other sleep-apnea treatment that cannot safely be withheld during OPIO2 research PSG nights.
  • Known severe pulmonary disease (e.g., advanced chronic obstructive pulmonary disease) that, in the opinion of the investigator, may increase the risk of oxygen-induced hypercapnia.
  • Unstable or clinically significant cardiopulmonary disease, including but not limited to decompensated heart failure, unstable angina, or clinically significant arrhythmia.
  • Recent hospitalization (within the past 30 days) or anticipated need for hospitalization during the study period.
  • Recreational or non-prescribed opioid use.
  • Alcohol use exceeding 2 standard drinks per day or evidence of substance use disorder that may interfere with study participation.
  • Presence of other sleep disorders or neurologic conditions that significantly affect breathing during sleep (e.g., neuromuscular disease), in the opinion of the investigator.
  • Pregnancy or breastfeeding, or planning to become pregnant during the study period.
  • Positive pregnancy test at screening (serum or urine) for participants able to become pregnant. A pregnancy test will be repeated before each awake chemoreflex session or in-laboratory PSG visit; one same-day test may cover both; a positive test triggers withdrawal from further study procedures.
  • Hospitalization for respiratory failure within the prior 12 months.
  • Severe untreated insomnia (Insomnia Severity Index >22) likely to preclude completion of in-laboratory PSG visits.
  • Inability to communicate in English sufficient for informed consent and study procedures, where a qualified interpreter consistent with UCSD HRPP policy is not available.
  • Inability to tolerate nasal cannula or study procedures.
  • Inability to provide informed consent or comply with study procedures.
  • Any medical, psychiatric, or social condition that, in the opinion of the investigator, would interfere with safe participation or interpretation of study results.
  • Prisoners or individuals who are involuntarily incarcerated.
  • Inability or unwillingness to comply with research-center oxygen-safety precautions, including restrictions on smoking, vaping, open flames, and other ignition sources near oxygen equipment.

In addition to the enrollment exclusion criteria, participants will be excluded from randomization if the following criterion is met:

• Evidence of significant hypercapnia, defined as transcutaneous carbon dioxide (TcCO2) >55 mmHg for >10 minutes during baseline polysomnography (PSG).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Sham Air Followed by Supplemental Oxygen

Participants will receive sham air during the first in-laboratory overnight polysomnography (PSG) visit, followed by an approximately 1-week washout period, and then receive supplemental oxygen during the second in-laboratory overnight PSG visit.

Sham air will be delivered during sleep through a nasal cannula using a standard wall air flow controller during an in-laboratory overnight polysomnography (PSG). Sham air will be delivered at a fixed flow rate of 4 L/min and may be reduced to 3 L/min for participant comfort.

Supplemental oxygen will be delivered during sleep through a nasal cannula using a standard wall oxygen flow controller during an in-laboratory overnight polysomnography (PSG). Supplemental oxygen will be delivered at a fixed flow rate of 4 L/min and may be reduced to 3 L/min for participant comfort.

实验性的:Supplemental Oxygen Followed by Sham Air

Participants will receive supplemental oxygen during the first in-laboratory overnight polysomnography (PSG) visit, followed by an approximately 1-week washout period. Participants will then receive sham air during the second in-laboratory overnight PSG visit.

Sham air will be delivered during sleep through a nasal cannula using a standard wall air flow controller during an in-laboratory overnight polysomnography (PSG). Sham air will be delivered at a fixed flow rate of 4 L/min and may be reduced to 3 L/min for participant comfort.

Supplemental oxygen will be delivered during sleep through a nasal cannula using a standard wall oxygen flow controller during an in-laboratory overnight polysomnography (PSG). Supplemental oxygen will be delivered at a fixed flow rate of 4 L/min and may be reduced to 3 L/min for participant comfort.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Flow-Based Apnea-Hypopnea Index (AHIflow)
大体时间:During each overnight intervention PSG, approximately 1 week apart

AHIflow is the number of apneas lasting at least 10 seconds plus airflow-reduction events with a greater than 30% reduction in airflow lasting at least 10 seconds, divided by total sleep time in hours. Each respiratory event is counted once. Oxygen desaturation or arousal is not required. AHIflow will be measured during each intervention PSG, and the primary treatment comparison will be the within-participant difference between the supplemental oxygen and sham air conditions.

During each overnight intervention PSG, approximately 1 week apart

次要结果测量

结果测量
措施说明
大体时间
Loop Gain
大体时间:During each overnight intervention PSG, approximately 1 week apart

Loop gain is a dimensionless measure of ventilatory control instability estimated from overnight polysomnography (PSG) data. Loop gain will be assessed during each intervention PSG to evaluate the effect of supplemental oxygen compared with sham air on ventilatory control.

During each overnight intervention PSG, approximately 1 week apart

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Jeremy Orr, MD、University of California, San Diego

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年12月1日

初级完成 (估计的)

2031年12月1日

研究完成 (估计的)

2031年12月1日

研究注册日期

首次提交

2026年10月16日

首先提交符合 QC 标准的

2026年11月2日

首次发布 (实际的)

2026年11月6日

研究记录更新

最后更新发布 (实际的)

2026年11月6日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

De-identified individual participant data generated under this protocol may be shared with collaborators or repositories, as permitted by the informed consent document, UC San Diego IRB/HRPP requirements, NIH/NHLBI data-sharing requirements, institutional policy, and applicable data-use agreements. Shared datasets will not include direct identifiers unless specifically approved by the IRB/HRPP and permitted by the informed consent document.

IPD 共享时间框架

Beginning after publication of the primary study results and available thereafter in accordance with NIH/NHLBI data-sharing requirements and applicable institutional policies.

IPD 共享访问标准

Qualified researchers may request access to de-identified individual participant data for research purposes. Access will be provided only as permitted by the informed consent document, UC San Diego IRB/HRPP requirements, NIH/NHLBI data-sharing requirements, institutional policy, and applicable data-use agreements. Shared datasets will not include direct identifiers unless specifically approved by the IRB/HRPP and permitted by the informed consent document.

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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