← Back to Clinical Trials
Recruiting NCT07554911

NCT07554911 Detection and Optimization of Treatment of Severe Cases of Dry Eye Disease

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07554911
Status Recruiting
Phase
Sponsor Singapore National Eye Centre
Condition Dry Eye
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2023-10-18
Primary Completion 2028-07-31

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 99 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 200 participants in total. It began in 2023-10-18 with a primary completion date of 2028-07-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: 1. 21 years old and above 2. Participants must be previously diagnosed with dry eye in the dry eye clinic (previous referred and had various forms of treatment such as artificial tears or prescription eyedrops) 3. Willing to perform all eye examinations and questionnaires in this study 4. Ability to provide informed consent Exclusion Criteria: 1. All subjects meeting any of the exclusion criteria at baseline will be excluded from participation and then list the criterion. 2. Any other specified reason as determined by clinical investigator

Contact & Investigator

Central Contact

Sharon Yeo, BSc

✉ sharon.yeo.w.j@singhealth.com.sg

📞 65767200

Principal Investigator

Louis Tong

PRINCIPAL INVESTIGATOR

Singapore Eye Research Institute (SERI)

Frequently Asked Questions

Who can join the NCT07554911 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 99 Years, studying Dry Eye. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07554911 currently recruiting?

Yes, NCT07554911 is actively recruiting participants. Contact the research team at sharon.yeo.w.j@singhealth.com.sg for enrollment information.

Where is the NCT07554911 trial being conducted?

This trial is being conducted at Singapore, Singapore.

Who is sponsoring the NCT07554911 clinical trial?

NCT07554911 is sponsored by Singapore National Eye Centre. The principal investigator is Louis Tong at Singapore Eye Research Institute (SERI). The trial plans to enroll 200 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology