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N/A N=527

DEXYCU (Dexamethasone Intraocular Suspension) 9% Retrospective Study 001

Cataract

Enrolled (actual)
527
Serious AEs
0.0%
Results posted
May 2021
Primary outcome: Primary: Percentage of Eyes With Anterior Chamber Cell Grade 0 — 65 percentage of eyes

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
DEXYCU (dexamethasone intraocular suspension) 9%. (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
EyePoint Pharmaceuticals, Inc.
Primary completion
May 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Eyes With Anterior Chamber Cell Grade 0
65

Summary

Retrospective study to provide clinical outcomes with DEXYCU (dexamethasone intraocular suspension) 9%.

Eligibility Criteria

Inclusion Criteria

  • Male and Female subjects at least 18 years of age
  • Subjects who underwent cataract surgery from 12Mar2019 to 15Dec2019 and received DEXYCU

Exclusion Criteria

  • Subjects who underwent cataract surgery and did not receive DEXYCU
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04290676). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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