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Obstructive Sleep Apnoea in Patients With Type 1 Diabetes

4. september 2020 oppdatert av: University of Birmingham

Obstructive Sleep Apnoea (OSA) in Patients With Type 1 Diabetes (T1D): A Cross-Sectional Study

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.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

Obstructive sleep apnoea (OSA) has been reported to be very common in patient with type 2 diabetes (T2D), and this relation is expected as both conditions share obesity as a common risk factor. Despite that several articles have stated that OSA is an independent risk factor for abnormal glucose metabolism, hypertension, and cardiovascular diseases.

In contrast, patients with type 1 diabetes (T1D) are leaner and younger than patients with T2D, so it was expected that OSA might be less common in patients with T1D. However, few studies have reported the prevalence of OSA in T1D with a range between 8 and 46%. The relationship between OSA and diabetes-related vascular disease is poorly explored in patients with T1D. This suggests a mechanism other than obesity may be responsible for OSA in patients with T1D. Therefore, the investigators hypothesized that (1) OSA is related to CAN rather than obesity in patients with T1D. (2) OSA is common in patients with T1D. (3) OSA is associated with worse metabolic profile and microvascular complications in T1D. (4) Oxidative and nitrosative stress are possible mechanisms relating OSA to T1D complication.

Studietype

Observasjonsmessig

Registrering (Faktiske)

47

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Birmingham, Storbritannia, B9 5SS
        • Birmingham Heartlands Hospital, Heart of England NHS Foundation Trust

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

The study population will be patients with type 1 diabetes attending secondary care diabetes clinics at Heart of England NHS Foundation Trust (HEFT) in Birmingham.

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The relationship between OSA and cardiac autonomic neuropathy (CAN) in patients with T1D.
Tidsramme: Single time point measurement (20- 30 min)

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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The prevalence of obstructive sleep apnoea in patients with T1D.
Tidsramme: Single time point measurement (over 8 hours) at participant residence
Sleep apnoea will be assessed using portable multi-channel home-based sleep device.
Single time point measurement (over 8 hours) at participant residence
The relationship between the presence of OSA and metabolic profile in patients with T1D.
Tidsramme: Single time point measurement (15 min)
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)
The relationship between OSA and the presence of microvascular complications in T1D patients.
Tidsramme: Single time point measurement (1-2 hours)
Microvascular complications include diabetic neuropathy, diabetic nephropathy, and diabetic retinopathy.
Single time point measurement (1-2 hours)
The potential mechanisms for the relationship between OSA and diabetic-related complications
Tidsramme: Single time point measurement (about 5 min)
Will be assessed using serum and plasma blood samples.
Single time point measurement (about 5 min)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Abd Tahrani, MD, NIHR Clinician Scientist at University of Birmingham

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

14. februar 2018

Primær fullføring (Faktiske)

27. juni 2019

Studiet fullført (Faktiske)

27. juni 2019

Datoer for studieregistrering

Først innsendt

5. mars 2018

Først innsendt som oppfylte QC-kriteriene

21. mars 2018

Først lagt ut (Faktiske)

29. mars 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

7. september 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. september 2020

Sist bekreftet

1. august 2020

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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