Galilei Lens Professional vs. Predicate Devices: a Comparison Study
Primary Purpose
Cataract
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Galilei Lens Professional
IOLMaster
Lenstar
Sponsored by
About this trial
This is an interventional diagnostic trial for Cataract
Eligibility Criteria
Inclusion Criteria:
- spherical equivalent between -10 D and +10 D
- best-corrected VA of 20/100 or better.
Exclusion Criteria:
- strabism
- blepharitis
- nystagmus
- amblyopia
- anisometropia (spherical equivalent > 1D)
- angle closure glaucoma
- seizure disorder
- brain damages
- Down syndrome
- trisomy 13 or 18
- cerebral palsy
- other serious disorders of the eye or central nervous systems
Sites / Locations
- Eye Clinic Orasis
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Experimental
Arm Label
Normal
Mild Cataract
Severe cataract
Arm Description
Arm: Normal eyes Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Arm: Eyes with mild cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Arm: Eyes with severe cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Outcomes
Primary Outcome Measures
Agreement With Predicate Devices in Terms of Agreement 1
Assessed parameters:
Axial Length (AL; G6, IOLM, LS) Central Corneal Thickness (CCT; G6, LS)) Anterior Chamber Depth (ACD; G6, IOLM, LS) Lens Thickness (LT; G6, LS) Corneal Curvature (SimK; G6, IOLM, LS) White-to-White (WtW; G6, IOL, LS)
Agreement With Predicate Devices in Terms of Agreement 2
Assessed Parameters:
Simulated Corneal Curvature (SimK; G6, IOLM, LS)
Secondary Outcome Measures
Agreement With Devices of the Same Type in Terms of Repeatability
Assessed parameters:
Axial Length (AL) Central Corneal Thickness (CCT) Anterior Chamber Depth (ACD) Lens Thickness (LT) Corneal Curvature (SimK) White-to-White (WtW)
Full Information
NCT ID
NCT01961089
First Posted
October 7, 2013
Last Updated
September 26, 2019
Sponsor
Ziemer Ophthalmic Systems AG
1. Study Identification
Unique Protocol Identification Number
NCT01961089
Brief Title
Galilei Lens Professional vs. Predicate Devices: a Comparison Study
Official Title
GALILEI Lens Professional vs. Predicate Devices: a Comparison Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ziemer Ophthalmic Systems AG
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study question: How does the new GALILEI Lens Professional compare to predicate devices? Study hypothesis: The GALILEI Lens Professional achieves a better precision in the postoperative, calculated target refraction with cataract surgeries than predicate devices, and it is more versatile in the measurable parameters as well as more user-friendly.
Detailed Description
Background: An accessory to the commercially available GALILEI Dual-Scheimpflug Corneal Topographer/Keratometer with the name "EBR Accessory" was developed by the company Ziemer Ophthalmic Systems AG for the measurement of intraocular distances. The combination is called "GALILEI Lens Professional". The measurement principle is based on on short coherence interferometry/-reflectometry, which has gained wide-spread application and has been applied clinically, including one of the members of this study group, for the precise measurement of axial, intraocular distances (12.1.). Such EBR Accessory measurements, in combination with measurements by the GALILEI, may be applied to given intra-ocular lens (IOL) types and IOL equations, an permit the calculation of suggested IOLs that are implanted during cataract surgery, in order to achieve the desired vision correction. To register this accessory for sale, the precision and agreement to existing devices with similar applications ("predicate devices") must be demonstrated. One complete measurement consists of a cornea-topography/keratometry scan, followed immediately by three consecutive, axial biometry scans of the anterior segment (cornea and crystalline lens) and - after a short re-alignment - three consecutive, axial biometry scans of the retina. The measurement process is continuous, but divided in two steps. Blinking by the patient is possible in between the two steps, which increases patient comfort and, in certain cases, measurement success. Precision is evaluated by three repeated, complete measurements with the GALILEI Lens Professional and each predicate device. Two standard devices with comparable optical technology that are used in routine cataract surgery were declared as predicate devices. These two devise are typically used in combination with standard keratometers, as which the GALILEI Lens Professional may be employed as well.
Goal: The comparison of the GALILEI Lens Professional to predicate devices with respect to precision in measuring postoperative, calculated target refractions in cataract patients, and versatility of measurable quantities.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Normal
Arm Type
Experimental
Arm Description
Arm: Normal eyes Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Arm Title
Mild Cataract
Arm Type
Active Comparator
Arm Description
Arm: Eyes with mild cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Arm Title
Severe cataract
Arm Type
Experimental
Arm Description
Arm: Eyes with severe cataract Interventions: Galilei Lens Professional, IOLMaster, Lenstar
Intervention Type
Device
Intervention Name(s)
Galilei Lens Professional
Intervention Description
Measurement device
Intervention Type
Device
Intervention Name(s)
IOLMaster
Intervention Description
Measurement device
Intervention Type
Device
Intervention Name(s)
Lenstar
Intervention Description
Measurement device
Primary Outcome Measure Information:
Title
Agreement With Predicate Devices in Terms of Agreement 1
Description
Assessed parameters:
Axial Length (AL; G6, IOLM, LS) Central Corneal Thickness (CCT; G6, LS)) Anterior Chamber Depth (ACD; G6, IOLM, LS) Lens Thickness (LT; G6, LS) Corneal Curvature (SimK; G6, IOLM, LS) White-to-White (WtW; G6, IOL, LS)
Time Frame
3 months
Title
Agreement With Predicate Devices in Terms of Agreement 2
Description
Assessed Parameters:
Simulated Corneal Curvature (SimK; G6, IOLM, LS)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Agreement With Devices of the Same Type in Terms of Repeatability
Description
Assessed parameters:
Axial Length (AL) Central Corneal Thickness (CCT) Anterior Chamber Depth (ACD) Lens Thickness (LT) Corneal Curvature (SimK) White-to-White (WtW)
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
spherical equivalent between -10 D and +10 D
best-corrected VA of 20/100 or better.
Exclusion Criteria:
strabism
blepharitis
nystagmus
amblyopia
anisometropia (spherical equivalent > 1D)
angle closure glaucoma
seizure disorder
brain damages
Down syndrome
trisomy 13 or 18
cerebral palsy
other serious disorders of the eye or central nervous systems
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bojan Pajic, MD
Organizational Affiliation
Eye Clinic Orasis
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eye Clinic Orasis
City
Reinach
State/Province
Aargau
ZIP/Postal Code
5734
Country
Switzerland
12. IPD Sharing Statement
Learn more about this trial
Galilei Lens Professional vs. Predicate Devices: a Comparison Study
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