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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06179355
Other study ID # 1727367365
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2023
Est. completion date January 1, 2024

Study information

Verified date October 2023
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare manually performed Astigmatic Keratotomy to femtosecond laser astigmatic keratotomy to manage corneal astigmatism more than three diopters after phacoemulsification.


Description:

create circumferential corneal incisions, following the limbal curvature, at 1-1.5 mm anterior to the limbus, manually and by using femtosecond laser to correct corneal astigmatism more than three diopters after phacoemulsification.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Possibility to have informed consent and attendance of all study visits. - Patients who have undergone conventional phacoemulsification at least one month ago. - Clear cornea. - Astigmatism more than 0.5 diopters. Exclusion Criteria: - Corneal opacity. - History of corneal surgery. - Thin cornea. - Astigmatism equal to or less than 0.5 diopters.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
manual astigmatic keratotomy
manual astigmatic keratotomy using a diamond knife
femtosecond laser astigmatic keratotomy
astigmatic keratotomy using femtosecond lase

Locations

Country Name City State
Egypt Faculty of Medicine, Assiut University Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary astigmatism (Keratometric reading) diopters of the astigmatism after the procedure measured by Pentacam three month
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