search
Back to results

Antioxidant Carbocysteine Treatment in Obstructive Sleep Apnoea Syndrome

Primary Purpose

Obstructive Sleep Apnoea

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Carbocysteine
Continuous Positive Airway Pressure
Sponsored by
Guangzhou Institute of Respiratory Disease
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnoea focused on measuring Obstructive sleep apnoea, Antioxidant, drug treatment, oxidative stress, Continuous Positive Airway Pressure

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male in an age range of 18 to 65 years
  2. Obstructive Sleep Apnoea with an Apnea Hypopnea Index (AHI) of greater than or equal to 15 confirmed by polysomnography
  3. The patient is able to provide consent
  4. The patient were not receiving therapy for sleep apnoea,such CPAP or surgery.

Exclusion Criteria:

  1. Inability to tolerate Carbocysteine or CPAP
  2. Treatment with CPAP or surgery prior to or at the time of enrolment
  3. presence of active acute or chronic infection
  4. Patients with unstable cardiovascular diseases (unstable angina, myocardial infarction, stroke, or transient ischemic attacks), neuromuscular diseases, chronic respiratory diseases, peripheral vascular disease
  5. Using of steroidal , nonsteroidal anti-inflammatory, vasodilators ,lipid-lowering drugs,or other medications that lower oxidative stress.
  6. Intake of central relevant drugs, sedatives, or other drugs which impair sleep
  7. Unwilling to participate in the study
  8. Participation in another clinical study in the past 4 weeks
  9. Shift worker

Sites / Locations

  • Guangzhou institute of respiratory disease

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Carbocysteine

Continuous Positive Airway Pressure

Arm Description

Carbocysteine , tablet ,250mg per one tablet , patients oral intake with 500mg .tid.(1500mg/day)

Continuous Positive Airway Pressure(CPAP),auto-CPAP(USA,Philips), patients use Nasal CPAP overnight.

Outcomes

Primary Outcome Measures

Change of polysomnography (PSG) parameters after oral intake of Carbocysteine treatment
The Carbocysteine group will oral intake of Carbocysteine 500mg,tid for 6 weeks.We will examine the compliance with the drugs by Recycling the rest of the tablets.We compare the improvement of PSG parameters,such as AHI ,oxygen desaturation index(ODI),oxyhemoglobin saturation.
Daytime sleepiness(EDS) after oral intake of Carbocysteine treatment
EDS is evaluated by Epworth Sleeping Scale(ESS) grade.ESS≥9 means EDS.The higher the ESS, the more daytime sleepiness they feel.
Change of Oxidative Stress after oral intake of Carbocysteine treatment
Biomarkers is measured from venous blood.The blood is collected in the morning .After centrifugation ,the supernatant was kept at -80 degree centigrade.

Secondary Outcome Measures

Evaluate efficacy of oral intake of Antioxidant Carbocysteine in comparison to Nasal continuous positive airway pressure (CPAP) treatment .
We will examine the compliance with CPAP device memory download.We will compare the two group by the PSG parameters ,ESS, and Biomarkers .

Full Information

First Posted
December 10, 2013
Last Updated
January 6, 2015
Sponsor
Guangzhou Institute of Respiratory Disease
search

1. Study Identification

Unique Protocol Identification Number
NCT02015598
Brief Title
Antioxidant Carbocysteine Treatment in Obstructive Sleep Apnoea Syndrome
Official Title
Comparison of Oral Intake of Antioxidant Carbocysteine and Nasal Continuous Positive Airway Pressure (CPAP) for Treating in Moderate and Severe Obstructive Sleep Apnoea Syndrome Patients : a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guangzhou Institute of Respiratory Disease

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Obstructive sleep apnoea syndrome (OSAS) is characterised by repeated episodes of upper airway occlusion during sleep.It can cause cycles of hypoxia reoxygenation. And it was postulated that intermittent hypoxia seems to resemble ischemia-reperfusion.Many study suggest that ischemia-reperfusion represents an oxidative stress causing increased generation of reactive oxygen species, especially superoxide anions.It is one of the most important mechanisms of cardiovascular diseases, including hypertension, coronary artery disease and cerebrovascular accident complication with OSAS.So many individuals approve OSAS is an Oxidative Stress disease. Continuous positive airway pressure (CPAP) is the first-line of treatment method in moderate/severe OSA.But poor adherence to CPAP treatment is very common.The failure rate with CPAP treatment is more than 50%.So we are searching a new treatment for that patients. Carbocysteine is a antioxidant.It can not only scavenges the free radicals but also replenishes glutathione(GSH)which is has double antioxidant capacity. However, Carbocysteine is cheaper than other which has double antioxidant capacity drugs,such as N-acetylcysteine.The purpose is to evaluate efficacy of oral intake of Antioxidant Carbocysteine witch can reduce oxidative stress and improve the symptom of OSAS.It recover the imbalance in the oxidant-anti-oxidant status may reduce cardiovascular abnormalities in Patients with OSAS.
Detailed Description
OSAS patients are required to fill in questionnaire.And Inflammation biomarkers and Oxidative Stress biomarkers and ultrasonic will be tested.Then patients are randomly allocated to one of two groups. One group is treated with oral intake of Antioxidant Carbocysteine 500mg tid. The second group is treated with CPAP. After 6 weeks treatment, all patients will take the overnight polysomnogram test again, and take questionnaire, blood , ultrasonic test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnoea
Keywords
Obstructive sleep apnoea, Antioxidant, drug treatment, oxidative stress, Continuous Positive Airway Pressure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Carbocysteine
Arm Type
Experimental
Arm Description
Carbocysteine , tablet ,250mg per one tablet , patients oral intake with 500mg .tid.(1500mg/day)
Arm Title
Continuous Positive Airway Pressure
Arm Type
Active Comparator
Arm Description
Continuous Positive Airway Pressure(CPAP),auto-CPAP(USA,Philips), patients use Nasal CPAP overnight.
Intervention Type
Drug
Intervention Name(s)
Carbocysteine
Other Intervention Name(s)
S-Carboxymethylcysteine; SCMC
Intervention Description
carbocisteine (2×250 mg, three times daily) for 6 weeks. The tablets are provided by Baiyunshan Pharmaceutical, China. patients will interviewed after 3 weeks to check their adherence to the study regimen by collecting and counting the number of remaining tablets, record adverse events, and refill study tablets for the next 3 weeks.
Intervention Type
Device
Intervention Name(s)
Continuous Positive Airway Pressure
Other Intervention Name(s)
Nasal Continuous Positive Airway Pressure
Intervention Description
Patients will interviewed after 3 weeks and the end of trial.We will check their compliance to device memory download , record adverse events and pressure .
Primary Outcome Measure Information:
Title
Change of polysomnography (PSG) parameters after oral intake of Carbocysteine treatment
Description
The Carbocysteine group will oral intake of Carbocysteine 500mg,tid for 6 weeks.We will examine the compliance with the drugs by Recycling the rest of the tablets.We compare the improvement of PSG parameters,such as AHI ,oxygen desaturation index(ODI),oxyhemoglobin saturation.
Time Frame
after 6 weeks
Title
Daytime sleepiness(EDS) after oral intake of Carbocysteine treatment
Description
EDS is evaluated by Epworth Sleeping Scale(ESS) grade.ESS≥9 means EDS.The higher the ESS, the more daytime sleepiness they feel.
Time Frame
after 6 weeks
Title
Change of Oxidative Stress after oral intake of Carbocysteine treatment
Description
Biomarkers is measured from venous blood.The blood is collected in the morning .After centrifugation ,the supernatant was kept at -80 degree centigrade.
Time Frame
after 6 weeks
Secondary Outcome Measure Information:
Title
Evaluate efficacy of oral intake of Antioxidant Carbocysteine in comparison to Nasal continuous positive airway pressure (CPAP) treatment .
Description
We will examine the compliance with CPAP device memory download.We will compare the two group by the PSG parameters ,ESS, and Biomarkers .
Time Frame
after 6 weeks treatment
Other Pre-specified Outcome Measures:
Title
Change of vascular function after oral intake of Antioxidant Carbocysteine
Description
Vasoreactivity Testing Protocol and intima-media thickness is measured by high-resolution ultrasonography at baseline and 6 weeks after treatment.Vasoactive mediators from blood will be studied.
Time Frame
after 6 weeks after oral intake of Carbocysteine treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male in an age range of 18 to 65 years Obstructive Sleep Apnoea with an Apnea Hypopnea Index (AHI) of greater than or equal to 15 confirmed by polysomnography The patient is able to provide consent The patient were not receiving therapy for sleep apnoea,such CPAP or surgery. Exclusion Criteria: Inability to tolerate Carbocysteine or CPAP Treatment with CPAP or surgery prior to or at the time of enrolment presence of active acute or chronic infection Patients with unstable cardiovascular diseases (unstable angina, myocardial infarction, stroke, or transient ischemic attacks), neuromuscular diseases, chronic respiratory diseases, peripheral vascular disease Using of steroidal , nonsteroidal anti-inflammatory, vasodilators ,lipid-lowering drugs,or other medications that lower oxidative stress. Intake of central relevant drugs, sedatives, or other drugs which impair sleep Unwilling to participate in the study Participation in another clinical study in the past 4 weeks Shift worker
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
NuoFu Zhang, professor
Organizational Affiliation
Guangzhou Institute of Respiratory Disease
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guangzhou institute of respiratory disease
City
Guangzhou,
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
26849119
Citation
Wu K, Su X, Li G, Zhang N. Antioxidant Carbocysteine Treatment in Obstructive Sleep Apnea Syndrome: A Randomized Clinical Trial. PLoS One. 2016 Feb 5;11(2):e0148519. doi: 10.1371/journal.pone.0148519. eCollection 2016.
Results Reference
derived

Learn more about this trial

Antioxidant Carbocysteine Treatment in Obstructive Sleep Apnoea Syndrome

We'll reach out to this number within 24 hrs