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SAS in Patients With Bronchial Carcinoma

Incidence of Sleep Apnea Syndrome (SAS) in Patients With Bronchial Carcinoma

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02270853
Acronym
SAS CA
Enrollment
100
Registered
2014-10-21
Start date
2014-04-30
Completion date
2016-12-31
Last updated
2016-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchial Carcinoma, Sleep Apnea Syndrome

Keywords

ApneaLink, bronchial carcinoma, sleep apnea screening

Brief summary

In this study it will be analyzed how often the sleep apnea syndrome can be observed in patients with newly diagnosed lung cancer with the help of ApneaLink device by ResMed.

Detailed description

Determination of the SAS- frequence in patients with bronchial carcinoma. The patients will be screened at home for 1 night with the ApneaLink device by ResMed. The apneaLink device is a standard screening tool for sleep apnea in clinical practice.

Interventions

DEVICEsleep apnea screening with ApneaLinkTM

ApneaLink is sleep-screening tool that objectively identifies patients with sleep apnea

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with reasonable suspicion of bronchial carcinoma or histologically proven bronchial carcinoma, which has not been medicated until the study entry and * Patients with sleep apnea who had recently been diagnosed with bronchial carcinoma.

Exclusion criteria

* Pregnancy * other already known malignancies or tumors * Patients with non-invasive artificial respiration due to a chronic respiratory insufficiencies

Design outcomes

Primary

MeasureTime frameDescription
percent of sleep apnea in patients with bronchial carcinomatwo daysThe percent of sleep apnea in a cohort of patients with bronchial carcinoma will be evaluated. The duration of the study participation is two days.

Countries

Germany

Contacts

Primary ContactAngela Habier
ahabier@ukaachen.de0492418037429

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026