The Necessity and Optimal Time for Performing Pars Plana Vitrectomy in Acute Retinal Necrosis Patients
1 other identifier
observational
30
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2012
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2017
CompletedFirst Submitted
Initial submission to the registry
August 21, 2017
CompletedFirst Posted
Study publicly available on registry
August 24, 2017
CompletedAugust 24, 2017
August 1, 2017
4.8 years
August 21, 2017
August 21, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
visual acuity
1 year
Secondary Outcomes (1)
retinal detachement
1 year
Study Arms (3)
1
there was no retinal detachment (RD) at the first visit. The group 1 patients were treated with systemic antiviral medications, as well as with intravitreal antiviral injections
2
there was no RD at the first visit. The group 2 patients were treated with systemic antiviral medications and PPV plus silicone oil tamponade and intravitreal injection.
3
there was RD at the first visit. The group 3 patients were treated with systemic antiviral medications and PPV plus silicone oil tamponade and intravitreal injection
Interventions
Eligibility Criteria
ARN patients
You may qualify if:
- ARN was diagnosed according to the American Uveitis Society Diagnostic Criteria (1994)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
August 21, 2017
First Posted
August 24, 2017
Study Start
April 1, 2012
Primary Completion
February 1, 2017
Study Completion
February 1, 2017
Last Updated
August 24, 2017
Record last verified: 2017-08
Data Sharing
- IPD Sharing
- Will not share