Repeatability and Reproducibility of the ArcScan Insight 100 VHF Digital Ultrasound

• Sponsor: London Vision Clinic (Other)
• Overall Status: Suspended
• CT.gov ID: NCT02519985
• Collaborator: Arcscan, Inc. (Industry)
• Enrollment: 40
• Location: 1
• Arm: 1
• Anticipated Duration (Months): 85.9
• Patients Per Site Per Month: 0.5

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the repeatability and reproducibility of corneal (including corneal, epithelial, stromal, and LASIK flap thickness) and anterior segment measurements using the ArcScan Insight 100 very high-frequency digital ultrasound arc-scanner.

Condition or Disease	Intervention/Treatment	Phase
Corneal Thickness Measurement; Epithelial Thickness Measurement; Anterior Eye Segment Measurements	Device: ArcScan Insight 100 very high-frequency digital ultrasound	N/A

Detailed Description

Very high-frequency (VHF) digital ultrasound was first used in 1993 to obtain images of the cornea (the window at the front of the eye) and anterior segment (the space behind the cornea including the iris and the lens). A commercially available instrument, called the Artemis 2, has been used in routine clinical practice since 2001. The Artemis 2 was CE approved as well as having FDA approval (the US equivalent of the CE mark).

The ArcScan Insight 100 VHF digital ultrasound scanner is a new instrument so does not yet have a CE mark. However, the ArcScan Insight 100 is an upgraded version of the Artemis 2, so any differences are improvements to components, but the measurement method remains essentially the same.

The aim of the study is to establish the repeatability (i.e. the variability in measurements taken by a single examiner during a single visit) and reproducibility (i.e. the variability in measurements taken in the same conditions between two examiners) of the ArcScan Insight 100 device for measuring corneal and anterior segment parameters.

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 40 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Diagnostic
• Official Title: Repeatability and Reproducibility of Corneal and Anterior Segment Measurements by ArcScan Insight 100 Very High-frequency Digital Ultrasound
• Actual Study Start Date: Nov 1, 2016
• Anticipated Primary Completion Date: Dec 31, 2023
• Anticipated Study Completion Date: Dec 31, 2023

Arms and Interventions

Arm

Intervention/Treatment

Experimental: Repeatability and Reproducibility of ArcScan Insight 100 For repeatability and reproducibility in normal eyes (n=20): Firstly, 5 consecutive repeated ArcScan Insight 100 scans of the cornea and anterior segment will be performed by the first operator. After a break of about 30 minutes, 5 consecutive repeated ArcScan Insight 100 scans of the cornea and anterior segment will be performed by the second operator. For repeatability and reproducibility in eyes after laser refractive surgery (n=20): Firstly, 5 consecutive repeated ArcScan Insight 100 scans of the cornea will be performed by the first operator. After a break of about 30 minutes, 5 consecutive repeated ArcScan Insight 100 scans of the cornea will be performed by the second operator.

Device: ArcScan Insight 100 very high-frequency digital ultrasound; The ArcScan Insight 100 VHF digital ultrasound scanner that can measure individual layers within the cornea with very high precision, as well as being able to image the interior of the eye including the chamber between the iris and the cornea, the lens and other structures behind the iris. The ArcScan Insight 100 device is a digital ultrasound scanner, meaning that it uses ultrasound waves to measure parameters of the eye. The Insight examination involves the patient sitting in front of the ultrasound unit and looking through a disposable goggle-like eyepiece at a light source. Warm sterile balanced saline solution (like natural tears) are used to fill the space between the light source and the eye, to allow ultrasound transmission. There is no contact between the instrument and the eye other than being immersed in this water bath.; Other Names: VHF digital ultrasound

Outcome Measures

Primary Outcome Measures

1. Repeatability of ArcScan Insight 100 corneal scans in normal eyes (standard deviation) [1 day]

   The standard deviation of 5 repeated measurements for corneal thickness, epithelial thickness, and stromal thickness in normal eyes with no previous corneal surgery

Secondary Outcome Measures

1. Reproducibility of ArcScan Insight 100 corneal scans in normal eyes (between-operator standard deviation) [1 day]

   The between-operator standard deviation of 5 repeated measurements for each operator for corneal thickness, epithelial thickness, and stromal thickness in normal eyes with no previous corneal surgery

2. Repeatability of ArcScan Insight 100 anterior segment scans in normal eyes (standard deviation) [1 day]

   The standard deviation of 5 repeated measurements for anterior segment dimensions: angle diameter, sulcus diameter, anterior chamber depth, and lens rise from the zonular plane in normal eyes with no previous corneal surgery

3. Reproducibility of ArcScan Insight 100 anterior segment scans in normal eyes (between-operator standard deviation) [1 day]

   The between-operator standard deviation of 5 repeated measurements for each operator for anterior segment dimensions: angle diameter, sulcus diameter, anterior chamber depth, and lens rise from the zonular plane in normal eyes with no previous corneal surgery

4. Repeatability of ArcScan Insight 100 corneal scans in eyes after corneal laser refractive surgery (standard deviation) [1 day]

   The standard deviation of 5 repeated measurements for corneal thickness, epithelial thickness, stromal thickness, flap thickness, and residual stromal thickness in eyes after corneal laser refractive surgery

5. Reproducibility of ArcScan Insight 100 corneal scans in eyes after corneal laser refractive surgery (between-operator standard deviation) [1 day]

   The between-operator standard deviation of 5 repeated measurements for each operator for corneal thickness, epithelial thickness, stromal thickness, flap thickness, and residual stromal thickness in eyes after corneal laser refractive surgery

Eligibility Criteria

Criteria

• Ages Eligible for Study: 21 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

INCLUSION CRITERIA Only patients who are medically suitable for corneal refractive surgery can be included in the study.

As general inclusion criteria the following aspects are defined:

• Subjects should be 21 years of age or older.

• Contact lens wearers must stop wearing their contact lenses at least four weeks per decade of wear before baseline measurements in case of hard contact lenses and one week before baseline measurements in case of soft contact lenses.

• Patient will be able to understand the patient information and willing to sign an informed consent.

For the repeatability and reproducibility phase using normal eyes of the study:

• Eyes with no ocular pathology

• Eyes with no previous ocular or corneal surgery

For the repeatability and reproducibility phase using post-LASIK eyes of the study:

• Eyes between 3 and 9 months after LASIK or SMILE

For the comparison of ArcScan Insight 100 VHF digital ultrasound with RTVue OCT

• Either eyes before or after corneal refractive surgery

EXCLUSION CRITERIA

• Previous ocular or corneal surgery (for normal eyes)

• Patient not being able to tolerate local or topical anesthesia

• Patient has active conjunctivitis or any active ocular infection or inflammation

• Patient has a corneal ulcer

• Patient has an open wound on the corneal epithelium

• Patient has compromised epithelium (e.g. ≥Grade 3 superficial punctate keratitis)

• Pregnancy

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	London Vision Clinic	London		United Kingdom	W1G 7LA

Sponsors and Collaborators

• London Vision Clinic
• Arcscan, Inc.

Investigators

• Principal Investigator: Dan Z Reinstein, MD MA, London Vision Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

• Ogbuehi KC, Osuagwu UL. Repeatability and interobserver reproducibility of Artemis-2 high-frequency ultrasound in determination of human corneal thickness. Clin Ophthalmol. 2012;6:761-9. doi: 10.2147/OPTH.S31690. Epub 2012 May 21.
• Paul T, Lim M, Starr CE, Lloyd HO, Coleman DJ, Silverman RH. Central corneal thickness measured by the Orbscan II system, contact ultrasound pachymetry, and the Artemis 2 system. J Cataract Refract Surg. 2008 Nov;34(11):1906-12. doi: 10.1016/j.jcrs.2008.07.013.
• Piñero DP, Plaza AB, Alió JL. Anterior segment biometry with 2 imaging technologies: very-high-frequency ultrasound scanning versus optical coherence tomography. J Cataract Refract Surg. 2008 Jan;34(1):95-102. doi: 10.1016/j.jcrs.2007.08.033.
• Reinstein DZ, Silverman RH, Raevsky T, Simoni GJ, Lloyd HO, Najafi DJ, Rondeau MJ, Coleman DJ. Arc-scanning very high-frequency digital ultrasound for 3D pachymetric mapping of the corneal epithelium and stroma in laser in situ keratomileusis. J Refract Surg. 2000 Jul-Aug;16(4):414-30. Erratum in: J Refract Surg 2001 Jan-Feb;17(1):4.
• Ursea R, Feng M, Urs R, RoyChoudhury A, Silverman RH. Comparison of artemis 2 ultrasound and Visante optical coherence tomography corneal thickness profiles. J Refract Surg. 2013 Jan;29(1):36-41. doi: 10.3928/1081597X-20121126-01. Epub 2012 Nov 30.

• Responsible Party: Dan Reinstein, Medical Director, London Vision Clinic
• ClinicalTrials.gov Identifier: NCT02519985
• Other Study ID Numbers: LoVC-005
• First Posted: Aug 11, 2015
• Last Update Posted: Apr 26, 2022
• Last Verified: Apr 1, 2022

• Keywords provided by Dan Reinstein, Medical Director, London Vision Clinic: VHF digital ultrasound; Corneal thickness; Epithelial thickness; Angle diameter; Sulcus diameter; Anterior chamber depth; Repeatability; Reproducibility

Study Results

No Results Posted as of Apr 26, 2022