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NCT04595357 Clinical Trial

"Iris Shelf" Technique for Intraocular Foreign Bodies Removal

Eye Injuries Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04595357
Other study ID # 17300500
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date July 1, 2020

Study information
Verified date October 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Intraocular foreign body (IOFB) injury is a common potentially serious form of ocular trauma. Metallic IOFB is the most common type of IOFB injury. Apart from the associated ocular tissue damage, Metallic IOFB may cause permanent visual impairment due to retinal toxicity and endophthalmitis. When presenting posteriorly, the approach of IOFB removal is challenging. Several techniques had been described for posterior IOFB removal. All of these techniques aimed to remove IOFB with the least possible collateral damage. This study aims to describe "Iris shelf" technique for posterior IOFB removal through a clear corneal incision combined with phaco-vitrectomy and report its outcomes.

Recruitment information / eligibility
Status Completed
Enrollment 33
Est. completion date July 1, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers
Gender All
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria: - posterior segment metallic IOFB who underwent combined phacovitrectomy with IOFB removal through a clear corneal incision using "Iris shelf" technique Exclusion Criteria: - Any other surgical technique for posterior segment IOFB removal

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Iris shelf technique
Removal of posterior segment intraocular foreign bodies through corneal incision combined with phaco-vitrectomy

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary corrected distance visual acuity 1 month
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