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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02784977
Other study ID # 09.2016.311
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 3, 2017
Est. completion date December 31, 2027

Study information

Verified date October 2022
Source Koç University
Contact Yüksel Peker, Prof
Phone +905443483866
Email yukselpeker26@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Primary aim of the TURKAPNE (The Turkish Sleep Apnea Database) study is to generate a cross-sectional nationwide database to define clinical and polysomnographic characteristics of the sleep apnea patients in Turkey. Associations of phenotypes of sleep apnea patients with metabolic and cardiovascular diseases as well as risk for traffic accidents will be explored as secondary aims. Impact of treatment of sleep apnea on metabolic and cardiovascular complications as well as compliance with positive airway pressure treatment will be further explored longitudinally.


Description:

All subjects undergoing sleep study for suspicion of obstructive sleep apnea will be registered in a web-based national database regarding: - Anthropometric data, educational status, driving licence, - Smoking and alcohol use - Comorbidities, and drug use - Questionnaires, excessive daytime sleepiness - Polygraphic and polysomnographic findings - Blood pressure measurements - If taken, blood glucose, lipids and other biochemical markers - If measured, lung function test results - If measured, echocardiography findings - Follow-up data regarding treatment modality and compliance


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date December 31, 2027
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Consecutive adult patients undergoing sleep study for suspicion of obstructive sleep apnea - Ability to read and speak - Signed informed consent. Exclusion Criteria: - subjects who use positive airway pressure - subjects with limited life expectancy due to advanced renal disease or uncontrolled malignancies - subjects with alcohol dependency

Study Design


Intervention

Device:
Positive Airway Pressure (PAP)
Treatment of OSA with PAP
Intraoral device (IOD)
Treatment of OSA with IOD
Procedure:
Uvuloplasty
Uvuloplasty
Other:
Conservative treatment
No active intervention

Locations

Country Name City State
Turkey Koç University Hospital Istanbul

Sponsors (17)

Lead Sponsor Collaborator
Koç University Afyon Kocatepe University School of Medicine, Afyon, Turkey, Baskent University Hospital, Istanbul, Turkey, Dicle University School of Medicine, Diyarbakir, Turkey, Diskapi Yildirim Beyazit Education and Research Hospital, Dokuz Eylul University, Ege University School of Medicine, Izmir, Turkey, Hitit University School of Medicine, Corum, Turkey, Istanbul Sureyyapasa Chest Diseases and Chest Surgery Training and Research Hospital, Istanbul University Cerrahpasa School of Medicine, Istanbul, Turkey, Kocaeli Education and Research Hospital, Kocaeli, Turkey, Marmara University, Namik Kemal University School of Medicine, Tekirdag, Pamukkale University School of Medicine, Denizli, Turkey, Suleyman Demirel University School of Medicine, Isparta, Turkey, Trakya University School of Medicine, Edirne, Turkey, Uludag University School of Medicine, Bursa, Turkey

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Peker Y, Basoglu ÖK, Firat H; TURKAPNE Study Group. Rationale and Design of the Turkish Sleep Apnea Database - TURKAPNE: A National, Multicenter, Observational, Prospective Cohort Study. Turk Thorac J. 2018 Jul;19(3):136-140. doi: 10.5152/TurkThoracJ.2018.18097. Epub 2018 Jul 1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Metabolic and cardiovascular diseases in obstructive sleep apnea phenotypes The association of sleep apnea severity indices such as Apnea-Hypopnea Index and Oxygen Desaturation Index during Rapid Eye Movement (REM) sleep and non-REM sleep with self-reported diabetes mellitus and cardiovascular diseases will be explored. Up to three years
Secondary Sex differences in obstructive sleep apnea phenotypes Possible sex differences in REM-dependent sleep apnea, positional sleep apnea and its association with metabolic and cardiovascular diseases will be explored Up to three years
Secondary Adherence to positive airway pressure treatment in obstructive sleep apnea Predictors of adherence to positive airway pressure treatment (defined as device usage at least 4 hours of night during at least 70% of study period) in obstructive sleep apnea Through study completion, an average of 7 years
Secondary Incidence of cardiovascular diseases and mortality Number of patients who have died or developed cardiovascular diseases Through study completion, an average of 7 years
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