Clinical trial Recruiting at 1 site Observational Ages 50 to 90

Exploring dry eye disease patterns after cataract surgery

Official title: Ocular Surface and Corneal Morphological Changes After the Cataract Surgery and Associations With Inflammatory Biomarkers

Run by Lithuanian University of Health Sciences · NCT06298890 · Data updated 2026-11-12

This study looks at how cataract surgery affects dry eye symptoms in patients aged 50 to 90 and tests if using artificial tears helps improve their comfort over time.

Quick facts

Study typeObservational
Ages50 Years to 90 Years
SexAll
Enrollment100 (estimated)
SponsorLithuanian University of Health Sciences
Academic / other
Locations1 site (Kaunas)
StatusRecruiting
StartedMarch 2024
Main results expectedMay 2026
Study endsSeptember 2027
Registry record updatedMarch 7, 2024
Trial IDNCT06298890 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are cataract patients aged 50 to 90 without prior ocular surface diseases or surgeries.

Probably not a fit

Patients with severe dry eye disease, glaucoma, diabetes, or other systemic conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the patterns of dry eye disease (DED) following cataract surgery, focusing on ocular surface changes, corneal morphology, and patients' subjective assessments of DED. It aims to correlate these factors with ocular surface inflammation and pain biomarkers, while also evaluating the effectiveness of artificial tears for lubrication during long-term follow-up. The study involves cataract patients aged 50 to 90 who have undergone uncomplicated phacoemulsification by a single experienced surgeon.

Why it matters

Potential benefit: If successful, this study could enhance understanding of dry eye disease post-cataract surgery and improve management strategies for affected patients.

How similar studies have gone: While there have been studies on dry eye disease, this specific approach focusing on post-cataract surgery patterns is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Cataract patients from 50 to 90 years old who underwent uncomplicated phacoemulsification performed by one (and same) experienced surgeon.
* Patients with no underlying ocular surface diseases (keratitis, keratoconjunctivitis and others).
* Patients who previously did not undergo any ophthalmic surgery.

Exclusion Criteria:

* Patient expressed his wish to not participate in the study or discontinue it when already enrolled.
* Severe dry eye disease diagnosed with OSDI/DEQ-5 and at least one of the following tests: TBUT less than 10 seconds, tear osmolarity higher than 308 mOsm/l or positive corneal staining.
* Glaucoma.
* Diabetes mellitus.
* Systemic connective tissue disease, autoimmune disease.
* Neurologic conditions including stroke, Bell's palsy, Parkinson's, trigeminal nerve dysfunction.
* Patients who underwent refractive surgery (LASIK or PRK).
* Contact lens users.
* One or more of the following concomitant medications: psychiatric medicines, antihistamines and/or hormonal replacement.
* Patients who are already regularly using topical drops or ointments.

Where it's running

  • Lithuanian University of Health Sciences
    Kaunas, Lithuania
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • See if TRYPTYR 0.003% helps dry eye symptoms and signs

    This study tests whether acoltremon 0.003% can improve symptoms and eye findings in adults with dry eye disease.

    Recruiting at 2 sites Scott & Christie and Associates, PC · Scottsdale, Arizona and 1 other locations · NCT07926594

  • Rotational Stability of the Acunex Vario Toric

    This study tests whether the Acunex Vario toric extended-depth-of-focus intraocular lens stays stable in rotation and effectively reduces astigmatism for people undergoing cataract surgery.

    Recruiting Vienna Institute for Research in Ocular Surgery · Vienna · NCT07925840

  • Anterior segment anatomy assessment with swept-source OCT in eye surgery patients

    This study tests whether swept-source OCT can detail front-eye anatomy in patients undergoing anterior segment eye surgery.

    Recruiting Nanfang Hospital, Southern Medical University · Guangzhou, Guangdong · NCT07903454

  • MiLOOP-assisted cataract surgery for dense cataracts

    In people with dense cataracts, this study tests whether using the miLOOP device during cataract surgery can protect corneal cells and reduce ultrasound energy, compared with standard surgery.

    Recruiting Universiti Kebangsaan Malaysia Medical Centre · Cheras, Kuala Lumpur · NCT07898007

  • Lacrifill to Help Prevent Post-Curgery Dry Eye After Cataract Surgery

    This study tests Lacrifill to see if it helps prevent dry eye symptoms after unilateral cataract surgery.

    Recruiting at 2 sites Phase 4 Eye Research Associates, LLC · Pittsburg, Kansas and 1 other locations · NCT07796178

  • BL1107 dosing for drying eye redness: finding the lowest effective amount

    This trial tests whether different doses of BL1107 can fully reduce conjunctival redness in people with dry eye disease, while keeping participants unaware of the dose they receive.

    Recruiting Phase 2 Bausch & Lomb Incorporated · Newport Beach, California · NCT07778888

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.