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NCT04627402: CONTE

Effects of Adding Triamcinolone Acetonide to Conbercept Treatment for Refractory Diabetic Macular Edema (CONTE)

Status unknown NA Last updated 17 November 2020
What this trial tests

NA trial testing Conbercept and TA in Diabetes Mellitus, Type 2 in 50 participants. Status unknown.

Timeline
12 November 2020
Primary endpoint
1 June 2021
31 December 2021

Quick facts

Lead sponsorZhongshan Ophthalmic Center, Sun Yat-sen University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment50
Start date12 November 2020
Primary completion1 June 2021
Estimated completion31 December 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Zhongshan Ophthalmic Center, Sun Yat-sen University

Who can join

18 and older, any sex, with Diabetes Mellitus, Type 2 or Macular Edema. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aimed to compare intravitreous conbercept alone with conbercept plus intravitreous triamcinolone acetonide in DME eyes which showed limited response to anti-VEGF treatment after one injection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Diabetes Mellitus, Type 2

Currently open trials in the same condition.

Other Zhongshan Ophthalmic Center, Sun Yat-sen 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/NCT04627402.

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