Corneal Thickness Changes in Patient Undergoing Dry Eye Managment

Status Not yet recruiting

Clinical Trial Summary

The purpose of this research is to the determine effect of dry eye and to compare the effect of artificial tears on central and peripheral corneal thickness.

Clinical Trial Description

In this randomized controlled trial, 96 eyes of females with dry eye will be recruited through random sampling. Dry eye assessments will be done including TBUT, Schirmer test 1, and OSDI questionnaire. 96 eyes will be divided into 3 groups (32 eyes each) and will be provided intervention which is Polyethylene Glycol 400 0.4%-Propylene Glycol 0.3%. , Dextran 0.1%Hypromellose 0.3%, and placebo(normal saline) through randomization by an unmasked investigator. Changes in central and peripheral corneal thickness will be evaluated by corneal topography. Patients will be evaluated at baseline, after 15 days, after 1 month, and re-evaluated after 1 month of cessation of treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04970329
Study type	Interventional
Source	University of Faisalabad
Contact	Komal Atta, mbbs
Phone	03224075007
Email	komal.atta@tuf.edu.pk
Status	Not yet recruiting
Phase	N/A
Start date	July 2021
Completion date	August 2021

View Details

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