Actively Recruiting

Age: 21Years - 99Years
All Genders
Healthy Volunteers
NCT07554911

Detection and Optimization of Treatment of Severe Cases of Dry Eye Disease

Led by Singapore National Eye Centre · Updated on 2026-05-01

200

Participants Needed

1

Research Sites

249 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The bulk of dry eye patients are found in the community. The lack of satisfactory protocols and confidence is a significant deterrent for practitioners to manage such patients, which may result in inaccurate referrals, and unhappy patients. Problems are compounded by comorbidities of dry eye, even if these are not diagnosed formally. Aligning with the healthcare strategy to move beyond healthcare to health, and beyond hospital care to community care, investigators propose that the confidence of primary carers be increased by using an image-based screening system. This study aim to determine the efficacy of this screening AI algorithm, a prototype, in addition to or instead of screening of dry eye using a simple DEQ-5 symptom questionnaire.

CONDITIONS

Official Title

Detection and Optimization of Treatment of Severe Cases of Dry Eye Disease

Who Can Participate

Age: 21Years - 99Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 21 years old and above
  • Previously diagnosed with dry eye in the dry eye clinic
  • Have received various forms of treatment such as artificial tears or prescription eyedrops
  • Willing to perform all eye examinations and questionnaires in this study
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Any subject meeting any exclusion criteria at baseline will be excluded
  • Any other reason as determined by the clinical investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Singapore Eye Research Institute

Singapore, Singapore, 169856

Actively Recruiting

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Research Team

S

Sharon Yeo, BSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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