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Modification of Chronic Inflammation by Inhaled Carbon Monoxide in Patients With Stable Chronic Obstructive Pulmonary Disease (COPD)

This study has been completed.
Stichting Astma Bestrijding, The Netherlands
Information provided by:
Groningen Research Institute for Asthma and COPD Identifier:
First received: July 21, 2005
Last updated: September 11, 2006
Last verified: July 2006
The purpose of this study is to determine whether carbon monoxide is effective in the treatment of stable COPD.

Condition Intervention Phase
Pulmonary Disease, Chronic Obstructive Drug: carbon monoxide Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: Modification of Chronic Inflammation by Inhaled Carbon Monoxide in Patients With Stable COPD

Resource links provided by NLM:

Further study details as provided by Groningen Research Institute for Asthma and COPD:

Primary Outcome Measures:
  • percentage of neutrophils in induced sputum

Secondary Outcome Measures:
  • methacholine provocation threshold
  • exhaled CO/NO
  • FEV1, FVC, RAW, sgaw
  • inflammatory parameters in sputum and blood
  • 8-isoprostane in exhaled breath

Estimated Enrollment: 20
Study Start Date: January 2005
Estimated Study Completion Date: March 2006
Detailed Description:

COPD is characterised by a chronic pulmonary inflammation and a shifted oxidant/antioxidant balance. The main cause of this inflammation is smoking. After smoking cessation, this inflammation and shifted oxidant/antioxidant balance continues. This causes an increased deterioration of lung function compared to healthy persons of matching age.

The ongoing inflammation appears to be relatively insensitive to corticosteroid therapy.

Until now, there is no therapy for this inflammation. Both in vitro and in vivo studies show that carbon monoxide has, besides an antioxidant capacity, anti-inflammatory properties. The aim of this trial is to study whether the inflammation can be reduced by inhalation of carbon monoxide.


Ages Eligible for Study:   40 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Men and women, age > 40 years. Women must be post-menopausal (i.e. at least one year must have passed after the last menstruation), surgically sterile or using acceptable contraceptives, as judged by the investigator.
  • A diagnosis of COPD according to the criteria of the American Thoracic Society (ATS); a disease state characterised by the presence of chronic airway obstruction due to chronic bronchitis (cough/sputum on most days a week for 3 months a year for at least two successive years); or emphysema.
  • FEV1 > 0.7 litres
  • FEV1/FVC ratio < 70% (equation retrieval system [ERS] equations)
  • A smoking history of > 10 pack years
  • Completely stopped smoking > 1 year ago
  • No upper or lower respiratory tract infection in the last 4 weeks
  • In a stable phase of COPD, as judged by the investigator
  • Signed and dated informed consent obtained before any study related procedures (including withdrawal of concomitant medication) are conducted

Exclusion Criteria:

  • Treatment with immune-modulating agents for any other disease
  • History of asthma; former diagnosis of asthma
  • Arterial oxygen tension (PaO2) < 8.0 kPa
  • Any significant other pulmonary disease or disorder (e.g. alpha1-antitrypsin deficiency, bronchiectasies), as judged by the investigator
  • Patients with other significant disease or disorder (like cardiovascular, gastrointestinal, liver, renal, neurological, musculoskeletal, endocrine, metabolic [including diagnosed diabetes], malignant, psychiatric, major physical impairment), which, in the opinion of the investigator may either put the patient at risk because of participation in the study; or may influence the results of the study, or the patient’s ability to participate in the study.
  • Patients unable to blow reproducable lung function measurements
  • Patients using medicine with anti-oxidant character like n-acetyl-cysteine.
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Please refer to this study by its identifier: NCT00122694

University Medical Center Groningen, Department of Pulmonary Diseases
Groningen, Netherlands, 9700RB
Sponsors and Collaborators
Groningen Research Institute for Asthma and COPD
Stichting Astma Bestrijding, The Netherlands
Principal Investigator: H AM Kerstjens, Prof., MD, PhD University Medical Center Groningen, Department of Pulmonary Diseases
  More Information

Publications automatically indexed to this study by Identifier (NCT Number): Identifier: NCT00122694     History of Changes
Other Study ID Numbers: METc2003.249
SAB 2004/024
Study First Received: July 21, 2005
Last Updated: September 11, 2006

Keywords provided by Groningen Research Institute for Asthma and COPD:
carbon monoxide
sputum induction
stable COPD

Additional relevant MeSH terms:
Carbon Monoxide
Lung Diseases
Pulmonary Disease, Chronic Obstructive
Chronic Disease
Respiratory Tract Diseases
Pathologic Processes
Lung Diseases, Obstructive
Disease Attributes
Molecular Mechanisms of Pharmacological Action
Neurotransmitter Agents
Physiological Effects of Drugs processed this record on August 18, 2017