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Completed

NCT Number: NCT01136239

The Effect of High Dose N-acetylcysteine on Airtrapping and Airway Resistance in Chronic Obstructive Pulmonary Disease (COPD) Patients

This study is to investigate the add-on effect of high dose NAC (600mg tablet twice daily) on reduction of airtrapping and airway resistance in stable COPD patients as well as to study it's effect in reducing exacerbation, improving exercise capacity and quality of life in stable COPD patients.

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Key information

Age range

40 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Medical Department

Hong Kong, China

About this study

Background: The mucolytic and antioxidant effects of N-acetylcysteine (NAC) may be of great value in treatment of COPD patients. However, previous studies fail to demonstrate the beneficial effect of NAC. This may be due to insufficient dose of NAC used as well as inadequate outcome parameters measured in the past studies.

Objective of study: This study is to investigate the add-on effect of high dose NAC (600mg tablet twice daily) on reduction of airtrapping and airway resistance in stable COPD patients as well as to study it's effect in reducing exacerbation, improving exercise capacity and quality of life in stable COPD patients.

Study design: Randomized double blinded placebo controlled trial in Kwong Wah Hospital

Methodology: Patients are recruited in Kwong Wah Hospital if they fulfill the spirometric criteria of COPD. Eligible subjects will be randomized into the treatment (NAC 600mg tablet twice daily) and placebo group after completion of run in period. NAC and placebo will be prescribed accordingly in addition to their usual therapy. Both patients and investigators are blinded about the group allocation. Baseline assessment will be done and patients will be followed up at 16th weeks and 52th week of the study.

During each follow-up visit, hyperinflation parameters like inspiratory capacity (IC) will be measured by plethysmography. Airway resistance will be measured by both plethysmography and impulse oscillometry machine. Exercise capacity (6 min walking distance) and quality of life are also recorded during each follow up.

The difference of the above parameters between the 2 groups (drug and placebo group) will be analyszed by the Repeated measures ANOVA test

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Spirometry diagnosed COPD with FEV1/FVC ratio less than 70% and FEV1 less than 80% predicted
  • clinically stable and exacerbation free in the past 4 weeks
  • history of at least one COPD exacerbation in the past one year

Exclusion criteria

  • patients allergic or intolerant to NAC
  • Recent use of NAC in the past one month
  • history of asthma, non COPD respiratory disorders like bronchiectasis, pneumoconiosis or any active pulmonary infection
  • patients on long term steroid
  • patients on long term oxygen therapy or non invasive ventilation

Treatment and study plan

N-acetycysteine (600mg twice daily)

Drug

N-acetycysteine (600mg twice daily) for one year

Placebo

Drug

Placebo (600mg twice daily)

Primary outcomes

  1. Airtrapping in COPD patients

    Time frame: At baseline (time 0 week)

    The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)

  2. Airtrapping in COPD patients

    Time frame: At 16th week

    The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)

  3. Airtrapping in COPD patients

    Time frame: At 52th Week

    The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)

Secondary outcomes

  1. Airway resistance in COPD patients

    Time frame: At baseline ( time 0)

    Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.

  2. Airway resistance in COPD patients

    Time frame: At 16th week

    Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.

  3. Airway resistance in COPD patients

    Time frame: At 52th week

    Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.

  4. Exercise capacity

    Time frame: At baseline ( time 0)

    Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist

  5. Exercise capacity

    Time frame: At 16th week

    Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist

  6. Exercise capacity

    Time frame: At 52th week

    Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist

  7. Quality of life

    Time frame: At baseline (time 0)

    Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist

  8. Quality of life

    Time frame: At 16th week

    Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist

  9. Quality of life

    Time frame: At 52th week

    Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist

  10. COPD exacerbation rate

    Time frame: At 52th week

    The number of COPD exacerbation (exacerbation was defined as 2 out of 3 of the following criteria; 1.increase in shortness of breath, 2. increase in sputum purulence or 3. increase in sputum volume) will be assessed and documented

Sponsors and collaborators

Lead sponsor

Kwong Wah Hospital

Other

Registry information

Official study title

The Effect of High Dose N-acetylcysteine on Airtrapping and Airway Resistance of Chronic Obstructive Pulmonary disease-a Double Blinded Randomized Placebo Controlled Trial

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Jun 3, 2010
Registry last updated
Apr 9, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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