Measuring the Changes of the Intraocular Pressure After Corneal Cross Linking Using Corvis CT

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-35
SponsorTanta University

About this trial

To evaluate the changes that occur in the intraocular pressure before and after corneal cross linking using Corvis CT.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients who will corneal cross linking for mild degree of keratoconus, age between 19 and 35 years old

Disqualifiers

Corneal scarring.

Previous corneal infections.

Minimum corneal thickness at the thinnest location less than 400 µm.

History of uveitis or ocular allergy.

Trial design

Design model

Single group

Treatments tested in this trial

  • Corvis Machine

    Device

    Measuring the intraocular pressure

Treatment groups

1 Participants
are divided into 1 treatment group
Group A: Measuring the intraocular pressure after cross linkingOther 1 intervention

Trial outcomes

Primary outcomes

1

Intraocular pressure will be measured by using Corvis CT before cross linking and one month after cross linking

Recording the intraocular pressure

Time frame
Through the end of the study in approximately one year

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: