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NCT03163641

Safety and Effectiveness of OBG vs.a Bandage Contact Lens for Large Corneal Epithelial Defects in Patients Post-PRK.

Completed NA Last updated 17 December 2020
What this trial tests

NA trial testing Acuvue Oasys in Corneal Epithelial Wound in 45 participants. Completed in 8 November 2018.

Timeline
5 August 2018
Primary endpoint
31 October 2018
8 November 2018

Quick facts

Lead sponsorEyegate Pharmaceuticals, Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment45
Start date5 August 2018
Primary completion31 October 2018
Estimated completion8 November 2018
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Eyegate Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 22 to 50, any sex, with Corneal Epithelial Wound. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, randomized (Reading Center), masked, controlled study in up to 45 subjects who have undergone bilateral PRK with epithelial removal using alcohol in a 9.0 mm well or trephine at the time of surgery to ensure consistency of the size of the ablation area.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Acuvue Oasys

Trials testing the same drug.

Other Eyegate Pharmaceuticals, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03163641.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing