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Effects of Temazepam in Patients With Chronic Pulmonary Obstructive Disease

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Temazepam
Sponsored by
Rijnstate Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, respiratory, sleep quality, temazepam, dyspnea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: diagnosis of COPD, GOLD 3 or 4 having subjective sleeping problems longer latency to falling asleep frequent arousals excessive daytime sleepiness clinical stable health for minimally 6 weeks Exclusion Criteria: usage of some sort of medication that influences sleep in any kind of way (like benzodiazepines, barbiturates, opiates, amfetamines) which can not be discontinued during the study period alcohol abuse hospitalisation 6 weeks or shorter before enrollment in the study hyperreactivity / allergy to benzodiazepines history of benzodiazepine-dependence myasthenia gravis obstructive sleep apnea syndrome (OSAS) severe liver failure age under 18 years participation in another study less than 6 weeks before enrollment COPD exacerbation less than 6 weeks before enrollment usage of oxygen supplementation at home

Sites / Locations

  • Rijnstate Hospital

Outcomes

Primary Outcome Measures

transcutaneous PCO2
transcutaneous PO2
Oxygen saturation

Secondary Outcome Measures

Respiratory Disturbance Index
Desaturation Index
MSLT
arterial PO2
arterial PCO2
Hypercapnic Ventilatory Response
total sleeping time
sleep latency
percentage REM- and nREM-sleep of total sleep time
number of arousals
number of apneas during sleep
number of hypopneas during sleep
Epworth Sleeping Score
Dyspnea Visual Analog Score

Full Information

First Posted
October 27, 2005
Last Updated
October 31, 2007
Sponsor
Rijnstate Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00245661
Brief Title
Effects of Temazepam in Patients With Chronic Pulmonary Obstructive Disease
Official Title
Effects of Temazepam on Dyspnea, Gas Exchange and Sleep Quality in Chronic Obstructive Pulmonary Disease.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2007
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Rijnstate Hospital

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effects of temazepam during sleep and in daytime on dyspnea, gas exchange and sleep quality in patients with chronic obstructive pulmonary disease. The study hypothesis is that temazepam does not produce any adverse respiratory effects during sleep in patients with COPD. In contrast, it may result in an beneficiary effect because it positively affects the sleep quality and sleep structure which may result in more alertness and less daytime sleepiness and less dyspnea during the day.
Detailed Description
Rationale: More than 50% of patients with chronic obstructive pulmonary disease (COPD) have sleep complaints characterised by longer latency to falling asleep, more frequent arousals and awakenings, generalised insomnia and/or excessive daytime sleepiness. Sleep disturbance seems to be more severe with advancing disease and substantially reduces patients' quality of life. The sleep complaints are due to dyspnea, chronic cough, sputum production, hypoxaemia and hypercapnia during the night. One of the available therapies for these patients is the prescription of hypnotics (like benzodiazepines). However, it is thought that in patients with COPD sleep medication may produce adverse respiratory effects due to suppression of the cerebral respiratory drive. In our practice, we never encounter any adverse respiratory effect of an hypnotic in patients with COPD. There have been several trials in COPD patients studying these potentially adverse effects. The results of these studies are inconsistent, relative older hypnotics are used and there are several methodological limitations. Furthermore, in none of these studies transcutaneous PCO2 or PO2 was monitored. Temazepam is nowadays the sedative of first choice in the medical treatment of sleep complaints. Aim: primary: studying the effects of temazepam on the respiratory function during daytime and at night in patients with severe COPD. Secondary: studying the effects of temazepam on the sleep quality and sleep structure and on the objective and subjective sleepiness during daytime and at night in patients with COPD. Study design: double blind, placebo-controlled, cross-over randomised clinical trial. Treatment: 10 mg temazepam or placebo during seven consecutive nights. Endpoints: Primary: difference in PtcCO2, PtcO2 and oxygen saturation during sleep after 1 week temazepam compared to placebo. Secondary: Respiratory Disturbance Index, Desaturation Index and Hypercapnic Ventilatory Response, percentage REM/nREM-sleep and total effective sleep time, Multiple Sleep Latency Test and the Epworth Sleeping Score.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD, respiratory, sleep quality, temazepam, dyspnea

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
14 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Temazepam
Primary Outcome Measure Information:
Title
transcutaneous PCO2
Title
transcutaneous PO2
Title
Oxygen saturation
Secondary Outcome Measure Information:
Title
Respiratory Disturbance Index
Title
Desaturation Index
Title
MSLT
Title
arterial PO2
Title
arterial PCO2
Title
Hypercapnic Ventilatory Response
Title
total sleeping time
Title
sleep latency
Title
percentage REM- and nREM-sleep of total sleep time
Title
number of arousals
Title
number of apneas during sleep
Title
number of hypopneas during sleep
Title
Epworth Sleeping Score
Title
Dyspnea Visual Analog Score

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of COPD, GOLD 3 or 4 having subjective sleeping problems longer latency to falling asleep frequent arousals excessive daytime sleepiness clinical stable health for minimally 6 weeks Exclusion Criteria: usage of some sort of medication that influences sleep in any kind of way (like benzodiazepines, barbiturates, opiates, amfetamines) which can not be discontinued during the study period alcohol abuse hospitalisation 6 weeks or shorter before enrollment in the study hyperreactivity / allergy to benzodiazepines history of benzodiazepine-dependence myasthenia gravis obstructive sleep apnea syndrome (OSAS) severe liver failure age under 18 years participation in another study less than 6 weeks before enrollment COPD exacerbation less than 6 weeks before enrollment usage of oxygen supplementation at home
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerben Stege, MD
Organizational Affiliation
Rijnstate Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter J de Bruijn, MD
Organizational Affiliation
Rijnstate Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Richard PN Dekhuijzen, Prof. PhD MD
Organizational Affiliation
UMC St. Radboud
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Frank JJ van den Elshout, PhD MD
Organizational Affiliation
Rijnstate Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Yvonne F Heijdra, PhD MD
Organizational Affiliation
UMC St. Radboud
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Marjo JT van de Ven, PhD MD
Organizational Affiliation
Rijnstate Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Petra JE Vos, PhD MD
Organizational Affiliation
Rijnstate Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Rijnstate Hospital
City
Arnhem
State/Province
Gelderland
ZIP/Postal Code
6800 TA
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
19910177
Citation
Stege G, Heijdra YF, van den Elshout FJ, van de Ven MJ, de Bruijn PJ, van Sorge AA, Dekhuijzen PN, Vos PJ. Temazepam 10mg does not affect breathing and gas exchange in patients with severe normocapnic COPD. Respir Med. 2010 Apr;104(4):518-24. doi: 10.1016/j.rmed.2009.10.022. Epub 2009 Nov 12.
Results Reference
derived
Links:
URL
http://www.alysis.nl/site/index_html
Description
sponsor's web site

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Effects of Temazepam in Patients With Chronic Pulmonary Obstructive Disease

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