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Validation and Reliability of Iris Cameras in Mucopolysaccharidoses

Validation and Reliability of Iris Recognition and Manual InfraRed Cameras Using Bespoke Image Analysis Software for the Quantification of Corneal Opacification in Mucopolysaccharidoses

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05354219
Enrollment
60
Registered
2022-04-29
Start date
2023-03-08
Completion date
2023-09-08
Last updated
2023-03-22

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

Conditions

Mucopolysaccharidoses

Brief summary

To assess the reliablity and validity of 2 new iris cameras in the assement of corneal opacification in mucopolysaccharidoses

Detailed description

The mucopolysaccharidoses (MPS) are a group of disorders resulting from accumulation of glycosaminoglycans within various tissues including the eye. This can result in visual loss from corneal opacification. The assessment of corneal opacification is extremely subjective and based on a clinician grading this during slit lamp examination. There can be a significant variability and can prove problematic particularly in clinical trials assessing if corneal opacification is affected by potential new treatments. The use of imaging could facilitate objective measurement of corneal clouding. A previous study using an iris camera and image analysis to provide a corneal opacification measure score (COM score) demonstrated that it can be used in children with MPS, however it still had limitations- as the system is fully automated, if certain conditions are not met an image is not captured. This can be an issue in younger children who may not be cooperative, and limited its use in younger patient populations. It is anticipated that these limitations can be addressed by employing a newer iris camera (IriShield MK2120UL). The new camera's advantage is that it takes images monocularly, therefore only the eye under question needs to be aligned. We will also assess a new manual system (IRcamNew) which takes images whenever the shutter is manually pressed. This would be useful in children who cannot fixate with one eye, and can also be used when the child is examined under general anaesthetic which is commonly done in paediatric ophthalmology. If proven to be comparable to the existing iris camera (IriscamOrig) in terms of validity and reliability, the added benefits of these new iris cameras can open its use in a wider range of patient populations - for instance, in paediatric clinical trials-, as well as allowing longitudinal tracking of corneal clouding from early childhood well into adulthood.

Interventions

OTHERImaging

Imaging with 3 iris cameras

Sponsors

Orchard Therapeutics
CollaboratorINDUSTRY
Manchester University NHS Foundation Trust
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Any patient aged 0-100 with MPS type I, type III, type IV and type VI. Type VII MPS patients may also be eligible. For the control group - Participants of any age currently being followed at MREH that have an eye condition unrelated to the cornea as established by clinical examination.

Exclusion criteria

* MPS II

Design outcomes

Primary

MeasureTime frameDescription
Comparison of reliability of images taken by two different operators using the two ne w iris cameras2 monthsBland altman plots to compare reliability between images and COM scores obtained by 2 different operators
Correlation of COM scores between two new iris cameras and IrisCamOrig2 monthsValidity will be assessed by comparing the COM scores generated by the new iris cams to the previously validated iris camera

Secondary

MeasureTime frameDescription
Comparison of clinical grading to COM score obtained by image analysis1 monthCompare clinical grading of corneal opacification on slit lamp by clinicians to corneal opacification measure generated by image analysis

Countries

United Kingdom

Contacts

Primary ContactJane Ashworth, MD
jane.ashworth@mft.nhs.uk0161 276 1234

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026