Iris shelf technique
ProcedureRemoval of posterior segment intraocular foreign bodies through corneal incision combined with phaco-vitrectomy
NCT Number: NCT04595357
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.
Looking for future studies?
Notify Me15 year–45 year
All sexes
Observational
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Removal of posterior segment intraocular foreign bodies through corneal incision combined with phaco-vitrectomy
Time frame: 1 month
Assiut University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04837534
Amblyopia, Brain Diseases
Bharatpur, Chitwan, Nepal
View Trial DetailsNCT01490593
Craniocerebral Trauma, Eye Diseases
London, Ontario, Canada
View Trial DetailsNCT02638025
Craniocerebral Trauma, Eye Diseases
View Trial DetailsNCT00598299
Craniocerebral Trauma, Eye Diseases
Taipei, Taiwan
View Trial Details