Nasal Obstruction in Sleep Apnea Patients Compared to the General Population
NCT ID: NCT01282125
Last Updated: 2017-03-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
217 participants
OBSERVATIONAL
2010-12-31
2016-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This study aims to compare nose obstruction prevalence in sleep apnea patients and the general population
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Virtual Surgery of the Upper Airways
NCT04829201
Effect on Sleep of Surgical Treatment of Severe Nasal Obstruction
NCT05582070
Obstructive Sleep Apnea (OSA) in Pulmonary Arterial Hypertension (PAH)
NCT01835080
Obstructive Sleep Apnea - Patient Specific Factors, Success Rate and Compliance
NCT02953028
The Role of the Nose in Snoring and Sleep Apnea
NCT03072173
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
sleep apnea
100 patients suffering from obstructive sleep apnea syndrome
No interventions assigned to this group
controls
100 subjects matching cases to age, sex, and body weight
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sorlandet Hospital HF
OTHER_GOV
Norwegian University of Science and Technology
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ståle S. Nordgård, MD PhD
Role: PRINCIPAL_INVESTIGATOR
Aleris/NTNU
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
St Olavs Hospital Trondheim University Hospital
Trondheim, , Norway
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Moxness MH, Bugten V, Thorstensen WM, Nordgard S, Bruskeland G. A comparison of minimal cross sectional areas, nasal volumes and peak nasal inspiratory flow between patients with obstructive sleep apnea and healthy controls. Rhinology. 2016 Dec 1;54(4):342-347. doi: 10.4193/Rhino16.085.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OSAS og nasalstenose
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.