Thick Cornea with High Back Elevation
Long Term Follow-up Study on Thick Cornea with High Back Elevation
1 other identifier
observational
40
0 countries
N/A
Brief Summary
To follow up cases of thick cornea with high back elevation by pentacam.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2025
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 14, 2025
CompletedFirst Posted
Study publicly available on registry
April 2, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
ExpectedApril 2, 2025
March 1, 2025
1 year
March 14, 2025
March 25, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Measurement of corneal thickness and back corneal elevation by pentacam device
The investigator will image the cornea to measure corneal thickness and back corneal elevation using the Pentacam device and follow up for cases of thick corneas with high back elevation at 3 months, 6 months, and 1 year.
Baseline
Interventions
we will follow up on cases of thick cornea with high back elevation
Eligibility Criteria
any age can interact with pentacam device
You may qualify if:
- Any patient can interact with pentacam. Both Genders: include both males and females. Patients with thick cornea (\>540 µm) with high back elevation.
You may not qualify if:
- Patients with any eye disease (significant cataract or unstable glaucoma)
- Uncontrolled external disease such as blepharitis , moderate to severe dry eye and allergy.
- Patient with ocular disease such as uveitis, post herpetic infection and corneal opacity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principle investigator
Study Record Dates
First Submitted
March 14, 2025
First Posted
April 2, 2025
Study Start
May 1, 2025
Primary Completion
May 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
April 2, 2025
Record last verified: 2025-03