IOP Fluctuations in Patients With Sleep Apnea With or Without Primary Open Angle Glaucoma Using Positive Airway Pressure
Primary Purpose
Sleep Apnea, Obstructive, Primary Open-angle Glaucoma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SENSIMED Triggerfish®
Sponsored by
About this trial
This is an interventional diagnostic trial for Sleep Apnea, Obstructive
Eligibility Criteria
Inclusion Criteria:
- Patients with a confirmed diagnosis of moderate to severe OSAS, determined by a RDI > 15 on PSG
- Patient has either POAG with controlled IOP or no glaucoma. Five of each will included in the study
- Patients under CPAP therapy
- Aged ≥ 18 years, of either sex
- Not more than 4 diopters spherical equivalent on the study eye
- Not more than 2 diopters cylinder equivalent on the study eye
- Have given written informed consent, prior to any investigational procedures
Exclusion Criteria:
- Sleep disorders other than OSAS
- Use of sleep medication
- Patients with history of intraocular surgery (including laser therapy) within the last 3 months
- Corneal or conjunctival abnormality hindering contact lens adaptation
- Severe dry eye syndrome
- Patients with allergy to corneal anesthetic
- Patients with contraindications for silicone contact lens wear
- Patients not able to understand the character and individual consequences of the investigation
- Participation in other clinical research within the last 30 days
Sites / Locations
- The New York Eye and Ear Infirmary
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Sensimed Triggerfish
Arm Description
Outcomes
Primary Outcome Measures
Relationship Between IOP Fluctuation Pattern With or Without CPAP Therapy in Patients With Moderate to Severe OSAS With or Without POAG
24-hour IOP fluctuation pattern recorded using Triggerfish in patients with moderate to severe OSAS.
using CPAP in patients with or without POAG
not using CPAP in patients with or without POAG
Secondary Outcome Measures
Relationship Between the 24-hour IOP Fluctuation Patterns and Physiologic Parameters
Heart rate and ocular pulsation rate during sleep:
using CPAP in patients with or without POAG
not using CPAP in patients with or without POAG
Effect After CPAP Removal on the IOP Pattern
IOP pattern immediately after CPAP removal upon waking in patients with or without POAG
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01560975
Brief Title
IOP Fluctuations in Patients With Sleep Apnea With or Without Primary Open Angle Glaucoma Using Positive Airway Pressure
Official Title
A Prospective, Explorative, Open Label Study to Assess the 24-hour Intraocular Pressure Fluctuation Profile Recorded With SENSIMED Triggerfish® in Patients With Moderate to Severe Obstructive Sleep Apnea Syndrome Using Continuous Positive Airway Pressure With or Without Primary Open Angle Glaucoma
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sensimed AG
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Sleep apnea is characterized by repetitive episodes of decreased or interrupted airflow in the upper airways during sleep. Obstructive sleep apnea syndrome (OSAS) is the most common sleep-related breathing disorder and is characterized by repeated partial or complete upper airway collapse, gasping episodes, daytime sleepiness and fatigue. Once suspected, the diagnosis is made on the basis of anamnesis and a polysomnography (PSG) using the so-called respiratory disturbance index (RDI) to grade OSAS. Standard therapy consists of continuous positive airway pressure (CPAP) during sleep to prevent upper airway collapse. The association between OSAS and glaucoma has been extensively studied, although a few reports have been non-confirmatory. OSAS has been associated with reduced ocular blood flow, leading to hypoxia and hypercapnia, and as such, may represent a risk factor for glaucomatous optic neuropathy. OSAS has also been related to loss of nycthemeral rhythm of intraocular pressure (IOP). In addition, CPAP has been reported to increase IOP when used during nighttime.
The purpose of this study is to investigate how IOP varies in time, particularly during sleep in OSAS patients with or without glaucoma, and if the IOP variations are associated with the use of CPAP. IOP fluctuations will be monitored with SENSIMED Triggerfish®, a portable investigational device using a contact lens sensor that monitors the IOP fluctuation continuously over 24-hours.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Primary Open-angle Glaucoma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sensimed Triggerfish
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
SENSIMED Triggerfish®
Intervention Description
Portable investigational device using a contact lens sensor that monitors the IOP fluctuation continuously over 24-hours
Primary Outcome Measure Information:
Title
Relationship Between IOP Fluctuation Pattern With or Without CPAP Therapy in Patients With Moderate to Severe OSAS With or Without POAG
Description
24-hour IOP fluctuation pattern recorded using Triggerfish in patients with moderate to severe OSAS.
using CPAP in patients with or without POAG
not using CPAP in patients with or without POAG
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Relationship Between the 24-hour IOP Fluctuation Patterns and Physiologic Parameters
Description
Heart rate and ocular pulsation rate during sleep:
using CPAP in patients with or without POAG
not using CPAP in patients with or without POAG
Time Frame
24-hours
Title
Effect After CPAP Removal on the IOP Pattern
Description
IOP pattern immediately after CPAP removal upon waking in patients with or without POAG
Time Frame
30 min
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a confirmed diagnosis of moderate to severe OSAS, determined by a RDI > 15 on PSG
Patient has either POAG with controlled IOP or no glaucoma. Five of each will included in the study
Patients under CPAP therapy
Aged ≥ 18 years, of either sex
Not more than 4 diopters spherical equivalent on the study eye
Not more than 2 diopters cylinder equivalent on the study eye
Have given written informed consent, prior to any investigational procedures
Exclusion Criteria:
Sleep disorders other than OSAS
Use of sleep medication
Patients with history of intraocular surgery (including laser therapy) within the last 3 months
Corneal or conjunctival abnormality hindering contact lens adaptation
Severe dry eye syndrome
Patients with allergy to corneal anesthetic
Patients with contraindications for silicone contact lens wear
Patients not able to understand the character and individual consequences of the investigation
Participation in other clinical research within the last 30 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Ritch, MD
Organizational Affiliation
The New York Eye and Ear infirmary
Official's Role
Principal Investigator
Facility Information:
Facility Name
The New York Eye and Ear Infirmary
City
New-York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
12. IPD Sharing Statement
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IOP Fluctuations in Patients With Sleep Apnea With or Without Primary Open Angle Glaucoma Using Positive Airway Pressure
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