The Necessity and Optimal Time for Performing Pars Plana Vitrectomy in Acute Retinal Necrosis Patients

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03260049

Enrollment

Registered

2017-08-24

Start date

2012-04-30

Completion date

2017-02-28

Last updated

2017-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Retinal Necrosis

Brief summary

The records of patients who were diagnosed with ARN between April 2010 and February 2017 were analyzed.A retrospective review of the treatment options and outcomes of the these patients was performed.

Interventions

PROCEDUREpars plana vitrectomy

pars plana vitrectomy

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* ARN was diagnosed according to the American Uveitis Society Diagnostic Criteria (1994)

Exclusion criteria

Design outcomes

Primary

Measure	Time frame
visual acuity	1 year

Secondary

Measure	Time frame
retinal detachement	1 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026