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Dry EyesNCT01991132

Validating the Diagnostic Accuracy of Mediview 2.0 Software as an Image Analysis Tool of Meibomian Glands

A study testing MediView 2.0 software in people with Dry Eyes, run by Singapore National Eye Centre at 1 site in Singapore.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Non-contact meibography is a useful tool in assessing the health of meibomian glands in patients. Instead of using normal light in contact meibography, non-contact meibography utilises infra-red (IR) light. Read more about this study

Who is it for?
Ages 21 to 90 yearsHealthy volunteers can take part
Conditions the study is for
Dry Eyes
What is being tested?
MediView 2.0 software
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteSingapore
Study dates
Dec 2013to Dec 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 90 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Healthy volunteers/ patients that are willing to participate in this study.

Who cannot join

  • Any other specified reason as determined by clinical investigator.

Trial locations and contacts

1 site in 1 country.

Singapore1 site
  • Singapore Eye Research Institute

    Singapore, Singapore, 168751

Other trials in Singapore

About this study

Non-contact meibography is a useful tool in assessing the health of meibomian glands in patients. Instead of using normal light in contact meibography, non-contact meibography utilises infra-red (IR) light. IR light is shined on patients' inverted eyelids and a special camera then allows visualisation of the structure of the meibomian glands, including the ducts and acini. Currently, images taken via non-contact meibography are manually analysed by a skilled clinician.

Knowledge of the health of meibomian glands is useful, especially in the diagnosis of Meibomian Gland Dysfunction (MGD). Studies have shown that MGD is one of the most common causes of evaporative dry eye.

Read more

Mediview 2.0 is a software that has been programmed to semi-automatically classify meibograph images taken via non-contact meibography. This software is collaboration with Shanghai MediWorks Precision Instruments Co., Ltd. The algorithm used was developed by a collaboration between Agency for Science, Technology and Research (A*STAR) and Singapore Eye Research Institute (SERI).

This current study aims to validate the diagnostic accuracy of Mediview 2.0 in assessing the health of meibomian glands of patients, against a trained clinician. We aim to recruit 100 participants for this study.

Once this software is found to be valid, a trained technician could be taught how to capture the images and hence leaving the doctors with more time to focus on clinical assessment and treatment instead. Therefore, this study has the potential to increase efficiency in the clinics.

Read the detailed description

Meibomian gland dysfunction (MGD) is a chronic abnormality of the meibomian glands and commonly characterized by terminal meibomian duct obstruction and/or qualitative or quantitative changes in the glandular secretion. This may result in alteration of the composition and functioning of the tear film lipid layer, and subsequently destabilisation of the tear film. Studies have shown that MGD is one of the most common causes of evaporative dry eye.

It is recommended that the diagnosis of MGD be made by assessing ocular symptoms, lid morphology, mebomian gland mass, gland expressibility, lipid layer thickness and meibography. In meibography, the structure of the meibomian glands, including the ducts and acini can be observed. Photographic documentation of the meibomian gland is also possible under specialised illumination techniques.

There are two types of meibography currently in use- contact meibography and non-contact meibography. Non-contact meibography is advantageous over contact meibography as it is more comfortable for patients. In non-contact meibography, the slit-lamp microscope is equipped with an IR charge-coupled (CCD) device video camera and an IR transmitting filter. During the procedure, IR light is projected onto the inverted eyelid of the subject and the image of the eyelid captured by a camera.

Currently, skilled clinicians analyse images obtained via non-contact meibography manually to determine the health of the patient's eyelid. Through a collaborative project between scientists from bioinformatics institute, A*STAR, Singapore (Dr Lee Hwee Kuan) and SERI, semi-automatic algorithms for classifying meibographs into healthy and unhealthy have been previously developed. The commercial partner for this project, Mediworks, China, has incorporated these algorithms into the Mediview 2.0 software. This software consists of modules for acquiring meibography images as well as for analysing these images. Provided a user draws the outline of the tarsal plate on the captured image, the software is able to classify images into two categories- Healthy and Unhealthy without the aid of a skilled clinician. A trained technician could be taught how to capture the images and hence leaving the doctor with more time to focus on clinical assessment and treatment.

However, the accuracy and reproducibility of this software should be validated against a clinical assessor just as in the original algorithms. We propose to recruit 50 healthy volunteers and 50 patients from SNEC clinics and from public.

Clinical importance Should this modality of imaging be shown to be repeatable, it can be incorporated into current protocol/workflow for assessment and monitoring of Meibomian Gland Dysfunction and treatment progress in our centre. The images captured in this project can also be used for validating further updates of the Mediworks software, since the hardware will remain unchanged in the future.

Study Objectives and Purpose The primary purpose is to validate Mediview 2.0 software as an objective tool in assessing the health of meibomian glands.

The specific aims include assessing a., the accuracy of Mediview 2.0 in classifying meibograph images (into Healthy and Unhealthy categories) and b., reproducibility of the classifications.

Study design:

Prospective study

Rationale:

Mediview 2.0 is a newly developed software and has yet been validated as a tool for assessment of the health of meibomian glands.

Methods:

Participants and target sample size 50 healthy volunteers and 50 patients aged 21 to 99 years will be recruited for this study. They are outpatients and accompanying relatives from the Singapore National Eye Centre. Permission would be sought from the attending doctors before subjects are being recruited. Informed written consent will be obtained from all participants.

Visit schedules One visit is required for participants. In general, they will not have to come for additional visits if they are recruited whilst on a scheduled clinical appointment for other reasons. In exceptional cases, if the meibography cannot be performed on the same day, participants would be given the option of coming on another suitable day for this study.

Duration of study:

12 months.

Procedures:

  1. Imaging of Meibomian Gland During the imaging of each eye, participants will be required to place their chins on a chin rest on the slit-lamp microscope. The upper eyelids of the participant will be in turn everted and an image of meibomian glands present on the eyelid will be captured. This is also performed for the lower eyelids. This is a non-invasive technique and the camera and IR lamp will not touch the patient. During each eversion of eyelid, optometrist will acquire 3 images at one time. Thereafter, Mediview 2.0 software will proceed to analyse the image into healthy and unhealthy glands. Throughout all measurements, all parameters of the meibographer, (such as light intensity, magnification of eyelid) will be kept constant.
  2. Analysis of Image of Meibomian Gland The images taken above will be exported and assessed by another optometrist who is unaware of the classification of the image by Mediview. This assessor will classify the images into healthy and unhealthy. Results between the Mediview 2.0 software and the optometrist will be assessed. Should there be any disagreement on the results, a 3rd clinician will be involved in the validation.

Statistical analysis:

  1. Comparison between software classification and human classification Cohen's kappa coefficient will be calculated to assess the agreement between these two ratings. For interpretation of the calculated statistic, we use recommendations from Landis and Koch, who characterized values < 0 as indicating no agreement and 0-0.20 as slight, 0.21-0.40 as fair, 0.41-0.60 as moderate, 0.61-0.80 as substantial, and 0.81-1 as almost perfect agreement.
  2. Comparison between the first and second software classifications Similarly we will use the kappa coefficient to evaluate the agreements between the first and second classifications made by the software.

Expected outcomes:

The classification of meibograph images from Mediview 2.0 should show good agreement with the assessment by the skilled clinician. Similarly classifications of the meibographs taken on the same day for the same eyes should show good agreement.

Potential problems No potential problems are expected for this study.

Conditions
Dry Eyes
Being tested
MediView 2.0 software
Keywords
Dry Eyes, Meibomian glands, Algorithm, MediView software
Medical subject headings
Dry Eye Syndromes

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MediView 2.0 softwareOther

Study groups in NCT01991132
Study groupRoleWhat they receive
MediView 2.0 softwareOtherNot described
Receives: Other: MediView 2.0 software

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To certify the accuracy of the software

    To validate the accuracy of Mediview 2.0 in classifying meibograph images (into Healthy and Unhealthy categories) and reproducibility of the classifications.

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Nov 2013 (estimated)
  2. Study startDec 2013
  3. Primary completionDec 2014
  4. Study completionDec 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01991132
Sponsor's protocol ID
R1059/74/2013
Other IDs
2013/737/A
Status last verified
Jun 2014
First submitted
11 Nov 2013
Last updated
20 May 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing MediView 2.0 software in people with Dry Eyes, run by Singapore National Eye Centre at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 May 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To certify the accuracy of the software (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 May 2015.

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