Type 1 Diabetes Clinical Trial
Official title:
Obstructive Sleep Apnoea (OSA) in Patients With Type 1 Diabetes (T1D): A Cross-Sectional Study
Verified date | August 2020 |
Source | University of Birmingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The primary aim of this study is to assess the relationship between obstructive sleep apnoea
(OSA) and cardiac autonomic neuropathy (CAN) in patients with T1D.
The secondary aims of this study are to assess: (1) the prevalence of OSA in patients with
T1D; (2) the relationship between OSA and metabolic parameters (such as glycaemic control,
blood pressure, lipids and weight) in patients with T1D; (3) the relationship between OSA and
diabetes-related microvascular complications (retinopathy, nephropathy, peripheral
neuropathy) in patients with T1D; and (4) the potential mechanisms for the relationship
between OSA and diabetic-related complications if such a relationship is found.
Status | Completed |
Enrollment | 47 |
Est. completion date | June 27, 2019 |
Est. primary completion date | June 27, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - T1DM patient aged 18 and above, who was diagnosed more than 4 years ago. - Able to give informed consent. - Has sufficient proficiency in English to verbally answer interview questions. Exclusion Criteria: - Past medical history of severe respiratory disorders including treated OSA. - Patients using oxygen supplements. - Patients with end-stage renal disease receiving dialysis. - Pregnancy. - Dementia. - End stage diseases with life expectancy below 6 months. - Patients with implantable devices - Patients with known atrial fibrillation |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Birmingham Heartlands Hospital, Heart of England NHS Foundation Trust | Birmingham |
Lead Sponsor | Collaborator |
---|---|
University of Birmingham | Heart of England NHS Trust |
United Kingdom,
Borel AL, Benhamou PY, Baguet JP, Halimi S, Levy P, Mallion JM, Pépin JL. High prevalence of obstructive sleep apnoea syndrome in a Type 1 diabetic adult population: a pilot study. Diabet Med. 2010 Nov;27(11):1328-9. doi: 10.1111/j.1464-5491.2010.03096.x. — View Citation
Golbidi S, Badran M, Ayas N, Laher I. Cardiovascular consequences of sleep apnea. Lung. 2012 Apr;190(2):113-32. doi: 10.1007/s00408-011-9340-1. Epub 2011 Nov 3. Review. — View Citation
Manin G, Pons A, Baltzinger P, Moreau F, Iamandi C, Wilhelm JM, Lenoble P, Kessler L, Kessler R. Obstructive sleep apnoea in people with Type 1 diabetes: prevalence and association with micro- and macrovascular complications. Diabet Med. 2015 Jan;32(1):90-6. doi: 10.1111/dme.12582. Epub 2014 Sep 25. — View Citation
Reutrakul S, Van Cauter E. Interactions between sleep, circadian function, and glucose metabolism: implications for risk and severity of diabetes. Ann N Y Acad Sci. 2014 Apr;1311:151-73. doi: 10.1111/nyas.12355. Epub 2014 Mar 14. Review. — View Citation
Schober AK, Neurath MF, Harsch IA. Prevalence of sleep apnoea in diabetic patients. Clin Respir J. 2011 Jul;5(3):165-72. doi: 10.1111/j.1752-699X.2010.00216.x. Epub 2010 Jun 30. — View Citation
Tahrani AA. Obstructive sleep apnea in patients with diabetes: implications for clinical practice. Diabetes Management. 2015; 5(6):511-23. doi: 10.2217/dmt.15.34.
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The relationship between OSA and cardiac autonomic neuropathy (CAN) in patients with T1D. | CAN will be assessed using heart rate variability (HRV) and spectral analysis. During this test blood pressure and electrocardiogram (ECG) and will be recorded while resting in a sitting down position and during certain manoeuvres that include deep breathing and Valsalva, and standing up. The Result of this outcome will be categorized into normal, borderline, or abnormal. This study is one visit only, and the total duration of the visit is 2-4 hours. The time frame below is the approximate time needed to collect each outcome data. |
Single time point measurement (20- 30 min) | |
Secondary | The prevalence of obstructive sleep apnoea in patients with T1D. | Sleep apnoea will be assessed using portable multi-channel home-based sleep device. | Single time point measurement (over 8 hours) at participant residence | |
Secondary | The relationship between the presence of OSA and metabolic profile in patients with T1D. | This outcome will be assessed by comparing the routine assessment results for patients with OSA to patients without OSA. | Single time point measurement (15 min) | |
Secondary | The relationship between OSA and the presence of microvascular complications in T1D patients. | Microvascular complications include diabetic neuropathy, diabetic nephropathy, and diabetic retinopathy. | Single time point measurement (1-2 hours) | |
Secondary | The potential mechanisms for the relationship between OSA and diabetic-related complications | Will be assessed using serum and plasma blood samples. | Single time point measurement (about 5 min) |
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