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NCT05372562

Risk Factors for the Recurrent Postoperative Macular Edema Treated With OZURDEX

Completed Last updated 12 May 2022
What this trial tests

trial in Macular Edema in 30 participants. Completed in 30 April 2022.

Timeline
1 July 2017
Primary endpoint
30 April 2022
30 April 2022

Quick facts

Lead sponsorPeking University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date1 July 2017
Primary completion30 April 2022
Estimated completion30 April 2022
Sites1 location across China

Conditions studied

Sponsor

Peking University

Who can join

Eligibility, any sex, with Macular Edema. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Patients who were diagnosed as postoperative CME and administrated with intravitreal OZURDEX injection were reviewed. Outcome will include best-corrected visual acuity (BCVA), intraocular pressure (IOP) and central macular thickness (CMT). Recurrent CME and corresponding treatments were recorded.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Recent Achievements and Perspectives in Smart Nano-in-Micro Platforms for Ocular Disease Treatment.
    Huang Y, Yan D, Ouyang W, Hu J, et al · · 2025 · cited 1× · PMID 40546796 · DOI 10.2147/ijn.s518643

Verify or expand the search:

Other recruiting trials for Macular Edema

Currently open trials in the same condition.

Other Peking University 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/NCT05372562.

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