Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Dry Eye
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Phase IV, non inferiority, controlled, open, comparative, multicenter clinical studyMasking: Double (Participant, Investigator)Masking Description: After signing the informed consent form (ICF), every subject will receive a coded patient number and will be assigned randomly to one of the investigation products.Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04702776
Collaborators
Not Provided
Investigators
Not Provided