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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00876980
Other study ID # HKCTR-676
Secondary ID
Status Completed
Phase N/A
First received March 23, 2009
Last updated October 15, 2013
Start date May 2008
Est. completion date February 2012

Study information

Verified date October 2013
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that obstructive sleep apnea (OSA) contributes to impaired glucose homeostasis and associated vasculopathy, and nCPAP treatment of OSA should improve glycemic control and vascular function in OSA patients with type II diabetes mellitus. This study aims to investigate the therapeutic effects of nCPAP on glycemic control and vascular function in patients with OSA and type II diabetes mellitus.


Description:

Obstructive sleep apnoea (OSA) has been reported to be common (17%) in patients with diabetes mellitus (DM). Both OSA and DM are highly associated with cardiovascular morbidity and mortality. There is growing evidence that OSA may trigger or worsen pre-existing adverse metabolic profile indicative of cardiovascular risk. Treatment of OSA with nasal Continuous Positive Airway Pressure (nCPAP) has been shown to reduce blood pressure and hence to reduce the risk of atherogenesis. In patients with DM, the therapeutic effect of nCPAP is still not known, it would be important to delineate any independent effect of OSA on DM and the therapeutic effect of nCPAP on glycemic control to reduce the long term risk of macrovascular and microvascular complications.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date February 2012
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 70 Years
Eligibility Inclusion Criteria:

1. Patients with type II DM on a stable medication regimen (on diet / oral hypoglycaemic agents / insulin injections)

2. Age 25 - 70 years

3. HbA1C > 7%

4. AHI >= 15

5. Able to give written informed consent

Exclusion Criteria:

1. Patients with severe co-existing illness or poor functional performance

2. Patients with peripheral vascular diseases, vasculitis / Raynaud's syndrome or thrombocytopenia

3. Sleep disorders other than OSA

4. Patients who refuse nCPAP treatment for OSA

5. Excessive sleepiness causing potential harm (e.g. driver)

6. HbA1C >=7%

7. Habitual drinker (defined as more than 3 times a week)

8. Pregnant or lactating women

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Device:
nasal Continuous Positive Airway Pressure
A standard treatment for OSA. A portable machine delivers positive pressure through a mask to the upper airway during sleep at night.

Locations

Country Name City State
Hong Kong Queen Mary Hospital, University Department of Medicine Pokfulam

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

References & Publications (1)

West SD, Nicoll DJ, Wallace TM, Matthews DR, Stradling JR. Effect of CPAP on insulin resistance and HbA1c in men with obstructive sleep apnoea and type 2 diabetes. Thorax. 2007 Nov;62(11):969-74. Epub 2007 Jun 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary HbA1C 3 months No
Secondary Fasting glucose & fructosamine microalbuminuria blood pressure lipids endothelial function 3 months No
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