Single Ring Optical Catheter illumination study in patients with obstructive Sleep Apnea during DISE

Single Ring Optical Catheter illumination study in patients with obstructive Sleep Apnea during DISE - OC during DISE

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON43702

Enrollment

Registered

2016-03-31

Start date

2017-01-27

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

sleepingdisorder with apnoeas

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy subjects: + 18 years and older;OSA patients: + 18 years and older + diagnosis with moderate or severe OSA (AHI>15) + scheduled to undergo DISE

Exclusion criteria

Exclusion criteria: Healthy subjects and OSA patients: - morphological nasal airway abnormalities prohibiting entry of both nostrils by the endoscope or catheter - nasal congestion prohibiting entry of both nostrils by the endoscope or catheter - patients with suspected sensitivity to light, e.g. patients who had photodynamic therapy -inability to provide informed consent - pregnancy

Design outcomes

Primary

Measure	Time frame
Visuality of light ring projection on airway wall, configuration change during collapse and separation between the light rings.	—

Secondary

Measure	Time frame
n.a.	—

Countries

Netherlands

Outcome results