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Effects of Temazepam in Patients With Chronic Pulmonary Obstructive Disease

Effects of Temazepam on Dyspnea, Gas Exchange and Sleep Quality in Chronic Obstructive Pulmonary Disease.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00245661
Enrollment
14
Registered
2005-10-28
Start date
2005-10-31
Completion date
2007-08-31
Last updated
2007-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, respiratory, sleep quality, temazepam, dyspnea

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.

Interventions

Sponsors

Rijnstate Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
transcutaneous PCO2
transcutaneous PO2
Oxygen saturation

Secondary

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

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026