NCT Number: NCT01768078
Interest of Intravitreal Corticotherapy as the First-line Treatment for Post-operative Endophthalmitis
One useful effect of early intravitreal corticotherapy is to diminish inflammatory complications after endophthalmitis, which may cause, at least in part, serious complications (retinal detachment, macular edema) which are, more than the infection, causes of the complications seen after acute endophthalmitis.
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Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
CHU de Besançon, Besançon, France
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- All patients male or female with no age limit
- Hospitalized for the diagnosis and treatment of acute endophthalmitis following cataract surgery
- Who had given their consent after being informed about intravitreal corticotherapy
Exclusion criteria
- Patients who refused or were unable to give their consent
- Prior intravitreal corticotherapy
Treatment and study plan
Intravitreal injection of antibiotics
ProcedurePrimary outcomes
-
Measure the evolution of visual acuity
Time frame: up to12 months
Sponsors and collaborators
Lead sponsor
Centre Hospitalier Universitaire Dijon
Other
Registry information
Official study title
Interest of Intravitreal Corticotherapy as the First-line Treatment for Post-operative Endophthalmitis.
Acronym: Endophtalmitis
Important dates
- Study start
- 2008
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- Jan 15, 2013
- Registry last updated
- Dec 27, 2018
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.