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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04546997
Other study ID # 1212/2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 10, 2019
Est. completion date December 30, 2019

Study information

Verified date September 2020
Source Federico II University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the retinal vascular features using optical coherence tomography angiography in patients that received ocular blunt trauma.


Description:

To investigate, using optical coherence tomography angiography, early retinal vascular features 48 hours after ocular trauma and to detect their changes during 6 months' follow up.

The optical coherence tomography angiography represents a novel and noninvasive diagnostic technique that allows a detailed analysis of retinal vascular features.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date December 30, 2019
Est. primary completion date December 25, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria:

- age older than 40 years

- diagnosis of previous ocular blunt trauma

- absence of previous ocular surgery, congenital eye disease, high myopia (>6 dioptres), actual or previous diagnosis of glaucoma, optic disc anomaly, macular or vitreoretinal diseases.

- absence of significant lens opacities, low-quality OCT and OCT-A images.

Exclusion Criteria:

- age younger than 40 years

- absence of previous ocular blunt trauma

- presence of previous ocular surgery, congenital eye disease, high myopia (>6 dioptres), actual or previous diagnosis of glaucoma, optic disc anomaly, macular or vitreoretinal diseases.

- presence of significant lens opacities, low-quality OCT and OCT-A images.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Optical Coherence Tomography Angiography
Patients underwent non-invasive, fast, diagnostic imaging technique (optical coherence tomography angiography)

Locations

Country Name City State
Italy University of Naples "Federico II" Naples

Sponsors (1)

Lead Sponsor Collaborator
Federico II University

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary The measurements of retinal vessel density in patients after ocular blunt trauma during 6 months's follow up To evaluate the changes in retinal vessel density in 18 patients, at baseline and 1, 3, 6 months after ocular blunt trauma, using optical coherence tomography angiography.
The parameter analyzed by optical coherence tomography angiography was: retinal vessel density
Six months
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