WithdrawnNot Applicable

Healing of Persistent Epithelial Defects

Stopped: No patients recruited

United States0Started 2015-03

Plain-language summary

The purpose of this study is to compare the relative efficacy of four different treatment modalities (i.e. aggressive lubrication, bandage contact lens, Ambiodisk amniotic membrane, Prokera amniotic membrane) in the healing of persistent corneal epithelial defects following retina surgery.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

3.1 Inclusion Criteria * Adults aged 18 and older (inclusive) at the time of study enrollment * Recent history of retina surgery * Presence of persistent epithelial defect 7 days or later after surgery * English speaking 3.2 Exclusion Criteria * Non-English speaking patients * Inability to incapacity to provide consent for the study * History of corneal epithelial or limbal stem cell disease

What they're measuring

Abscence of persistent epithelial defect

Timeframe: 22 days

Trial details

NCT IDNCT02395952

SponsorMilton S. Hershey Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-02

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