Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2015-03-31
2018-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Lubrication
carboxymethylcellulose sodium
frequent topical lubrication with artificial tears
Bandage Contact Lens
Acuvue Oasys Contact Lens
Acuvue Oasys Bandage Contact Lens
Prokera
Wet amniotic membrane mounted on plastic retaining ring
Prokera
Ambiodisk
Freeze dried amniotic membrane
Ambiodisk
Interventions
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carboxymethylcellulose sodium
frequent topical lubrication with artificial tears
Acuvue Oasys Bandage Contact Lens
Ambiodisk
Prokera
Eligibility Criteria
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Inclusion Criteria
* Recent history of retina surgery
* Presence of persistent epithelial defect 7 days or later after surgery
* English speaking
Exclusion Criteria
* Inability to incapacity to provide consent for the study
* History of corneal epithelial or limbal stem cell disease
18 Years
ALL
Yes
Sponsors
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Milton S. Hershey Medical Center
OTHER
Responsible Party
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Seth M Pantanelli
Assistant Professor of Ophthalmology
Locations
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Penn State Hershey Eye Center
Hershey, Pennsylvania, United States
Countries
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Other Identifiers
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STUDY00001309
Identifier Type: -
Identifier Source: org_study_id
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