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Comparative Efficacy of Lipid Based Artificial Tears vs Aqueous Based Artificial Tears in Managing EDE

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated July 15, 2025 (before its estimated July 20, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Eligibility criteria revisedv3
  2. Primary endpoints: 4 to 5
    • Primary completion date: Jun 20, 2025 to Jul 20, 2025
    • Study description expanded, about 14 words
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This research aimed to compare the effectiveness of a lipid-based artificial tear (Recuro) against an aqueous-based artificial tear (Softeal) in managing EDE symptoms and signs.
Trial Details
NCT Number NCT06913387
Lead Sponsor Superior University
Conditions
(from sponsor)		 Evaporative Dry Eye
Related terms Dry Eye Syndromes
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov