search
Back to results

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

Primary Purpose

COPD

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
N-acetycysteine (600mg twice daily)
Placebo
Sponsored by
Kwong Wah Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COPD focused on measuring COPD, N-acetylcysteine, airtrapping, airway resistance, antioxidant

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Medical Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

N-acetylcysteine

Arm Description

Placebo (600mg twice daily)

N-acetylcysteine (600mg twice daily)

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Airway resistance in COPD patients
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Airway resistance in COPD patients
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Airway resistance in COPD patients
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Exercise capacity
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Exercise capacity
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Exercise capacity
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Quality of life
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
Quality of life
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
Quality of life
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
COPD exacerbation rate
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

Full Information

First Posted
June 1, 2010
Last Updated
April 8, 2015
Sponsor
Kwong Wah Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01136239
Brief Title
The Effect of High Dose N-acetylcysteine on Airtrapping and Airway Resistance in Chronic Obstructive Pulmonary Disease (COPD) Patients
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
February 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kwong Wah Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
COPD, N-acetylcysteine, airtrapping, airway resistance, antioxidant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
133 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo (600mg twice daily)
Arm Title
N-acetylcysteine
Arm Type
Active Comparator
Arm Description
N-acetylcysteine (600mg twice daily)
Intervention Type
Drug
Intervention Name(s)
N-acetycysteine (600mg twice daily)
Intervention Description
N-acetycysteine (600mg twice daily) for one year
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo (600mg twice daily)
Primary Outcome Measure Information:
Title
Airtrapping in COPD patients
Description
The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)
Time Frame
At baseline (time 0 week)
Title
Airtrapping in COPD patients
Description
The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)
Time Frame
At 16th week
Title
Airtrapping in COPD patients
Description
The airtrapping of COPD patients is measured by inspiratory capacity (IC), using plethsmography (MedGraphics Elite series)
Time Frame
At 52th Week
Secondary Outcome Measure Information:
Title
Airway resistance in COPD patients
Description
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Time Frame
At baseline ( time 0)
Title
Airway resistance in COPD patients
Description
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Time Frame
At 16th week
Title
Airway resistance in COPD patients
Description
Airway resistance is measured by plethsmography (Medgraphics Elite series) and impulse oscillometry.
Time Frame
At 52th week
Title
Exercise capacity
Description
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Time Frame
At baseline ( time 0)
Title
Exercise capacity
Description
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Time Frame
At 16th week
Title
Exercise capacity
Description
Exercise capacity is measured by 6-min-walking distance (6MWD)and it is performed by a trained physiotherapist
Time Frame
At 52th week
Title
Quality of life
Description
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
Time Frame
At baseline (time 0)
Title
Quality of life
Description
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
Time Frame
At 16th week
Title
Quality of life
Description
Quality of life is assessed by using the St Qeorge Respiratory Questionnaire (SQRQ)and it will be performed by a trained physiotherapist
Time Frame
At 52th week
Title
COPD exacerbation rate
Description
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
Time Frame
At 52th week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hoi Nam Tse, FHKAM, MBChB
Organizational Affiliation
Kwong Wah Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical Department
City
Hong Kong
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
24833327
Citation
Tse HN, Raiteri L, Wong KY, Ng LY, Yee KS, Tseng CZS. Benefits of high-dose N-acetylcysteine to exacerbation-prone patients with COPD. Chest. 2014 Sep;146(3):611-623. doi: 10.1378/chest.13-2784.
Results Reference
derived
PubMed Identifier
23348146
Citation
Tse HN, Raiteri L, Wong KY, Yee KS, Ng LY, Wai KY, Loo CK, Chan MH. High-dose N-acetylcysteine in stable COPD: the 1-year, double-blind, randomized, placebo-controlled HIACE study. Chest. 2013 Jul;144(1):106-118. doi: 10.1378/chest.12-2357.
Results Reference
derived

Learn more about this trial

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

We'll reach out to this number within 24 hrs