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Taking people in TürkiyeNo phase

TURKAPNE - The Turkish Sleep Apnea Database: A National, Multicenter, Observational, Prospective Cohort Study

Key facts

Who runs it
Koç University
Where
Istanbul, TürkiyeSee the site
Trial code
Status
Recruiting
People taking part
10,000 people, planned
Started
3 Oct 2017
Expected to end
31 Dec 2027
Type of study
Observational, 2 groups
Treatments tested
  • Positive Airway Pressure (PAP)
  • Intraoral device (IOD)
  • Uvuloplasty
  • Conservative treatment
Record updated
13 October 2022

Who can take part

Age
18 years to 80 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 6 criteriaShow less

Who can take part

  • Consecutive adult patients undergoing sleep study for suspicion of obstructive sleep apnea
  • Ability to read and speak
  • Signed informed consent

Who cannot take part

  • subjects with limited life expectancy due to advanced renal disease or uncontrolled malignancies
  • subjects who use positive airway pressure
  • subjects with alcohol dependency

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Where in Türkiye

  • Koc University HospitalIstanbul, TürkiyeContact: YÜKSEL PEKER, MD, PhD, ProfTaking people

About the trial

What the trial wants to find out

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.

The 2 groups in the trial

  • Obstructive Sleep Apnea (OSA)

    Patients with apnea hypopnea index of at least 5 events per hour. Intervention with positive airway pressure, or intraoral device, or uvuloplasty, or conservative treatment.

    Treatment: Positive Airway Pressure (PAP), Intraoral device (IOD), Uvuloplasty, and Conservative treatment

  • No-OSA

    Patients with apnea hypopnea index less than 5 events per hour. No intervention.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Fit questions
Built from NCT02784977, who can take part
Publications
Record updated
13 October 2022