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OpenTrials
Completed

NCT Number: NCT04464083

IOP Measurements Using ORA After ACXL in Keratoconus

The investigators measured IOP by Goldmann applanation tonometry(GAT) before and 6 months after accelerated 8 minutes CXL in using Avedro Kxl ,and correlated with corneal resistance factor(CRF)using ORA, AC angle and CCT using Scheimpflug imaging.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fayoum University

Al Fayyum, Egypt

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • KC patient indicated for CXL

Exclusion criteria

  • Advanced KC Glaucoma patients

Treatment and study plan

IOP Measurment

Diagnostic Test

To determine IOP readings before and after accelerated corneal collagen crosslinking (CXL)

Primary outcomes

  1. To determine IOP readings before and after accelerated corneal collagen crosslinking

    Time frame: April-October 2020

Sponsors and collaborators

Lead sponsor

Fayoum University

Other

Registry information

Official study title

Intraocular Pressure Measurements Using Ocular Response Analyzer After Accelerated Corneal Collagen Crosslinking With Riboflavin and Ultraviolet A in Keratoconus

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jul 9, 2020
Registry last updated
Feb 3, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.