Evaluation of Central Corneal Thickness in Patients With Vernal Keratoconjunctivitis Using Topical Steroids
NCT06913790 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 34
Last updated 2025-04-06
Summary
This prospective observational cohort study aims to assess changes in central corneal thickness (CCT) in vernal keratoconjunctivitis (VKC) patients using topical steroids. Data will be collected from tertiary care hospitals such as Al-Mustafa eye hospital and Jinnah Hospital, Lahore.
Conditions
- Vernal Keratoconjunctivitis
Sponsors & Collaborators
-
Superior University
lead OTHER
Eligibility
- Min Age
- 5 Years
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-03-20
- Primary Completion
- 2025-06-20
- Completion
- 2026-02-20
Countries
- Pakistan
Study Locations
More Related Trials
-
Impact of Scleral Contact Lens Wear on Corneal Nerves in Keratoconus
NCT03091101 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Visual Performance With Contact Lenses
NCT03705130 ·Status: COMPLETED
-
A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects
NCT02066922 ·Status: COMPLETED ·Phase: NA
-
An Investigation of the Impact of Localized Topical Anesthesia of the Ocular Surface on End-of-day Contact Lens Discomfort
NCT03733899 ·Status: COMPLETED ·Phase: NA
-
A 6-Hour Clinical Evaluation of New Daily-Wear Soft Contact Lenses
NCT03235089 ·Status: COMPLETED ·Phase: NA
-
Corneal and Conjunctival Sensitivity and Staining Study
NCT00455455 ·Status: COMPLETED ·Phase: PHASE4
-
Daily Wear Comparison of Enhanced and Non-Enhanced Silicone Hydrogel Lenses
NCT00813982 ·Status: COMPLETED ·Phase: NA
-
Overall Performance of a 1-day Silicone Hydrogel Lens When Habitual Soft Lens Wearers Are Refit
NCT02588573 ·Status: COMPLETED ·Phase: NA
-
Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance.
NCT00938951 ·Status: COMPLETED ·Phase: NA
-
Treating Contact Lens Discomfort With Orthokeratology
NCT03566680 ·Status: COMPLETED ·Phase: NA
-
In Vivo Measurement of Corneal Epithelial Changes in Dry Eye Patients
NCT01483989 ·Status: COMPLETED ·Phase: NA
-
Assessment of Corneal Endothelium After Collagen Cross Linking
NCT04160338 ·Status: UNKNOWN
-
Comparative Efficacy of Lipid Based Artificial Tears vs Aqueous Based Artificial Tears in Managing EDE
NCT06913387 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Investigation of Multi-Purpose Solution-Based Corneal Staining and Ocular Comfort
NCT00349843 ·Status: COMPLETED ·Phase: PHASE4
-
Ocular Effects of Scleral Lens Wear on Dry Eye Patients
NCT05079321 ·Status: COMPLETED ·Phase: NA
-
To Evaluate the Performance of Total 30 (Lehifilcon A) Contact Lenses in Patients Using Digital Devices for Greater Than 8 Hours Per Day 5 Days Per Week Based on Subjective Reported Data.
NCT06317038 ·Status: COMPLETED ·Phase: NA
-
Changes in the Tear Film With Scleral Contact Lens Wear for Keratoconic Eyes
NCT02806921 ·Status: COMPLETED ·Phase: NA
-
Multi-Centre Clinical Evaluation Of Two Daily Disposable Contact Lenses
NCT01707238 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of the Causes of Contact Lens Related Dry Eye
NCT00995189 ·Status: COMPLETED ·Phase: NA
-
Influence of Silicone Hydrogel Contact Lens Neophyte Wear on Corneal Sensitivity
NCT05745220 ·Status: COMPLETED ·Phase: NA
-
Novel Multifocal Soft Contact Lens Study
NCT06172881 ·Status: COMPLETED ·Phase: NA
-
Performance of Fanfilcon A Toric Lenses After at Least One Month Wearing Enfilcon A Toric Lenses
NCT02921412 ·Status: COMPLETED ·Phase: NA
-
Clinical Assessment of a Daily Wear Monthly Replacement Silicone Hydrogel Toric Contact Lens
NCT05211739 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of a Silicone Hydrogel Lens
NCT01016132 ·Status: COMPLETED ·Phase: NA
-
Visual Outcomes for Toric Efficacy Study
NCT03728218 ·Status: COMPLETED ·Phase: NA