Mass Spectral Fingerprinting in Obstructive Sleep Apnoea

See also
Status	Clinical Trial	Phase
Completed	`NCT02012868` - Effect of Bariatric Surgery on Obstructive Sleep Apnea in a Danish Cohort
Completed	`NCT01575210` - Assessment of the Performance of a New Reduced Noise Mask Vent	N/A
Completed	`NCT02050425` - Breath Analysis in Obstructive Sleep Apnoea	N/A
Active, not recruiting	`NCT04142905` - Is Asthma in Subjects With Obstructive Sleep Apnoea (OSA) Due to Dysanapsis

See also

Status

Clinical Trial

Phase

Completed

NCT02012868 - Effect of Bariatric Surgery on Obstructive Sleep Apnea in a Danish Cohort

Completed

NCT01575210 - Assessment of the Performance of a New Reduced Noise Mask Vent

N/A

Completed

NCT02050425 - Breath Analysis in Obstructive Sleep Apnoea

N/A

Active, not recruiting

NCT04142905 - Is Asthma in Subjects With Obstructive Sleep Apnoea (OSA) Due to Dysanapsis

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02810158
Study type	Observational
Source	University of Zurich
Contact
Status	Completed
Phase
Start date	June 2016
Completion date	May 2018

Mass Spectral Fingerprinting in Obstructive Sleep Apnoea

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms