Effect of Zopiclone on Compliance With Continuous Positive Airway Pressure in Obstructive Sleep Apnea

Sponsor
OSR Medical Inc. (Industry)
Overall Status
Completed
CT.gov ID
NCT01369576
Collaborator
(none)
264
4
2
42.1
66
1.6

Study Details

Study Description

Brief Summary

The clinical population targeted will be newly diagnosed patients with polysomnographically diagnosed OSA who are not currently taking hypnotics for concomitantly diagnosed insomnia. Outpatients who are also judged to be capable to follow the study procedures (consent, timelines, visits, questionnaires) and who do not have any concurrent disease that in the view of the investigator will interfere with participation in the trial to completion will be included. Approximately 160 subjects were recruited (80 per treatment arm) in the recent trial of eszopiclone. This size is expected to be able to discern an important difference of 80 minutes per night. In the current clinical population newly prescribed CPAP at Mount Sinai Hospital, the average compliance after 4 weeks of initiation of nCPAP was 4:01 (SD 2:59) hours per night. To be able to discern a difference of at least 1 hour (60 minutes) in usage per night, including entirely non-adherent patients who do not use treatment at all as 'zero hour' users, would require randomization of 264 patients (132 per group).

Our hypothesis for this study is that initial titration of CPAP treatment of OSA may be improved by initial prescription of a common hypnotic, zopiclone. To answer this question we intend to recruit 264 consecutive consenting subjects with OSA confirmed by a physician (ABSM or by a respirologist with extensive sleep medicine experience) with supportive polysomnography results who are willing to initiate long-term CPAP treatment.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

Background: Obstructive sleep apnea (OSA) is a common sleep breathing disorder that is associated with serious complications. Continuous positive airway pressure (CPAP) is the treatment of choice for most patients but its use in the real world is limited by low patient adherence which may result in sub-optimal outcomes for some patients. A single hypnotic with low risk of adverse effects is a cost-effective intervention to augment the currently low adherence to CPAP, especially if only prescribed for a limited time. The hypnotic is generic zopiclone 3.75-7.5 mg at bedtime for up to 14 doses.

The clinical population targeted will be newly expert physician-diagnosed patients polysomnographically supported OSA who are not currently taking hypnotics for concomitantly diagnosed insomnia. Outpatients who are also judged to be capable to follow the study procedures (consent, timelines, visits, questionnaires) and who do not have any concurrent disease that in the view of the investigator will interfere with participation in the trial to completion will be included.

Study Design

Study Type:
Interventional
Actual Enrollment :
264 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Double-blind, Randomized, Parallel Group Study to Determine the Effect of Initial Prescription of Zopiclone on the Level of Compliance With CPAP in Adult Patients Treated for OSA at 26 Weeks
Study Start Date :
May 1, 2011
Actual Primary Completion Date :
May 1, 2014
Actual Study Completion Date :
Nov 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

Usual sleep apnea and CPAP care Sleep apnea OSR Medical Treatment Plan©

Drug: Placebo
3.75-7.5mg 14 doses 4 weeks

Experimental: zopiclone

Sleep apnea OSR Medical Treatment plan ©

Drug: Zopiclone
3.75-7.5mg 14 doses 4 weeks

Outcome Measures

Primary Outcome Measures

  1. CPAP adherence [6 months]

Secondary Outcome Measures

  1. ESS and SAQLI scores, changes from baseline, % time of average CPAP usage over the last month/ self-estimated total sleep time (h). Residual AHI monitored, analysed for similar findings at trial closure and analysis, but is not an efficacy parameter [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • MD diagnosis of obstructive sleep apnea

  • No previous use of CPAP

  • No concurrent use of hypnotic medication

Exclusion Criteria:
  • Fatal comorbidities (i.e., life expectancy less than 6 months)

  • Contraindications for CPAP use

  • Pregnancy

  • Liver Failure

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cite de la Sante Laval Quebec Canada H7M 3L9
2 Institut de medecine specialisee de Laval Laval Quebec Canada H7S 2M5
3 Institut de Medecine du sommeil Montreal Quebec Canada H4N 1C5
4 Mount Sinai Hospital Montreal Quebec Canada H4W 1S7

Sponsors and Collaborators

  • OSR Medical Inc.

Investigators

  • Principal Investigator: Paul Verschelden, MD DABSM, Cite de la Sante, University of Montreal, OSR Medical, Institut de medecine specialisee de Laval (IMSL)
  • Principal Investigator: Marcel Baltzan, MDCM DABSM, McGill University, OSR Medical, Institut de medecine du sommeil (IMS)
  • Principal Investigator: Kateri Champagne, MD DABSM, McGill University Health Centre (MUHC), OSR Medical, Institut de medecine du sommeil (IMS)
  • Principal Investigator: Germaine Tanzimat, RN, OSR Medical Inc.
  • Principal Investigator: Barbara Capozzolo, MSc, OSR Medical Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
OSR Medical Inc.
ClinicalTrials.gov Identifier:
NCT01369576
Other Study ID Numbers:
  • OSRM-0511
First Posted:
Jun 9, 2011
Last Update Posted:
Jul 17, 2015
Last Verified:
Jul 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 17, 2015