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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03450213
Other study ID # Keratoconus
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2019
Est. completion date October 1, 2021

Study information

Verified date October 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Keratoconus is a bilateral (but usually asymmetrical) non-inflammatory progressive thinning process of the cornea. It manifests as characteristic cone-like ectasia of the cornea associated with irregular stromal thinning, resulting in a cone-like bulge , which causing irregular astigmatism and vision impairment.


Description:

Keratoconus is the most common form of corneal ectasia, with an incidence of 50-230 per 100,000 persons.Pentacam used diagnose & detect the progression in patients with keratoconus and also provide a detailed information about corneal tomography and topography.

In the last few years, it has been shown that in healthy individuals the posterior corneal surface has not only a different amount of astigmatism but also a different alignment of the steep meridian.

The aim of this research is to compare the amount and axis alignment of anterior and posterior corneal astigmatism in keratoconus with a healthy controlled group .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date October 1, 2021
Est. primary completion date October 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients diagnosed with keratoconus using the following criteria:

Specific diagnostic signs is asymmetric refractive errors with high progressive or irregular astigmatism, and elevated keratometry values, scissoring of the red reflex, Vogt striae, Fleischer rings, inferior or central steepening on topography with abnormal localized steepening .

Exclusion Criteria:

- Unwillingness to participate in the study .

- Corneal scarring.

- Any ectatic conditions that were not explicitly keratoconus such as keratoglobus and pellucid marginal degeneration .

- Previous ocular surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Pentacam
Pentacam will be used to measure the magnitude and axis orientation of anterior and posterior corneal astigmatism.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

References & Publications (1)

Rabinowitz YS. Keratoconus. Surv Ophthalmol. 1998 Jan-Feb;42(4):297-319. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison between astigmatism in patients with keratoconus and normal people. Pentacam will be used for comparison between astigmatism in patients with keratoconus and normal people at the same age and sex Two years
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