Measuring the Changes of the Intraocular Pressure After Corneal Laser Refractive Surgery Using Different Techniques
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 after corneal refractive surgery either PRK , LASIK and femtosecond laser by using Corvis CT results and applanation tonometer
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age between 19 and 35 years old
Myopia range from (-2.00 to -6.00 Diopter) .
Disqualifiers
Kertoconus.
Corneal scarring.
Previous corneal infections.
Minimum corneal thickness at the thinnest location less than 400 µm.
Trial design
Design model
Single group
Treatments tested in this trial
Corvis machine
Other interventionMeasuring intraocular pressure by different methods and compare the results
Treatment groups
50 Participants
are divided into 1 treatment groupGroup A: Measuring intraocular pressure by using different techniquesExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Measuring intraocular pressure
Intraocular pressure will be measured by in mmHg and by two methods : Corvis CT and applanation tonometer for each patient and will be recorded
Time frame
-The data collected will be before that laser surgery and one month after surgerySponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: