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

NAActive, not recruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

March 20, 2025

Primary Completion Date

July 20, 2025

Study Completion Date

February 20, 2026

Conditions
Evaporative Dry Eye
Interventions
COMBINATION_PRODUCT

Lipid Based Artificial Tears

30 participants received lipid-based artificial tears (Recuro) in this study arm. The intervention involved the administration of RECURO EYE DROPS, which contain Sodium carboxymethylcellulose 0.5%. Participants were instructed to instill 1-2 drops in each eye, three times daily (morning, afternoon, and evening) throughout the 6-week trial period.

COMBINATION_PRODUCT

Aqueous Based Artificial Tears

30 participants received aqueous-based artificial tears (Softeal) in this study arm. The intervention involved the administration of SOFTEAL EYE DROPS, which contain Hydroxypropylmethyl Cellulose 0.3%. Participants were instructed to instill 1-2 drops in each eye, three times daily (morning, afternoon, and evening) throughout the 6-week trial period.

Trial Locations (1)

Unknown

Mughal eye Hospital Johar town, Lahore

All Listed Sponsors
lead

Superior University

OTHER