Evaluation of the Effectiveness of Three Tear Substitute Formulations in Postoperative Discomfort After Cataract Surgery
Starting soon
Conditions studied: Cataract, Dry Eye
In brief
The primary objective of this study is the assessment of three tear substitute formulations in terms of postoperative discomfort following cataract extraction surgery by means of phacoemulsification and intraocular lens implantation.
Key facts
- Study ID
- NCT07581548
- Run by
- Democritus University of Thrace
- People needed
- 300
- Starts
- 2026-05-01
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2026-05-12
Who can join
Age: 45 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of senile cataract with stage 2 or 3 nuclear opalescence according to the - Lens Opacities Classification System III (LOCS-3) grading scale
You may not qualify if…
- Former incisional surgery
- Former diagnosis of corneal disease
- Autoimmune diseases
- Mental diseases
Where it is running
- University Hospital of Alexandroupolis — Alexandroupoli, Evros, Greece
Full record on ClinicalTrials.gov
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