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Clinical Trials in China / NCT06951087
Enrolling by invitation Phase 3

Intravitreal and Intracameral DEX in NPDR

NCT06951087 · tracked via the Priya Life Science China tracker
Sponsor
Affiliated Hospital of Nantong University
Phase
Phase 3
Started
2022-01-31
Last updated
2025-04-30

Condition(s) studied

Non-Proliferative Diabetic Retinopathy

Investigational drug(s) / intervention(s)

Dexamethasone sodium phosphate

Dexamethasone sodium phosphate: In patients with stable DR and no significant macular edema, intravitreal anti-VEGF injections after phacoemulsification surgery can prevent the worsening of postoperative macular edema and potentially improve final visual outcomes while maintaining safety. Laser coagulation and intravitreal anti-VEGF injections are currently considered the standard treatments for PDR. However, the cost of anti-VEGF drugs often prevents many patients from receiving regular and timely injections. Intravitreal corticosteroids may be used as an alternative to anti-VEGF agents.

Study summary

To investigate the effects of intravitreal and intracameral injection of dexamethasone during cataract phacoemulsification in patients with mild to moderate non-proliferative diabetic retinopathy

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: type 2 diabetic cataracts patients who were diagnosed with mild to moderate NPDR Exclusion Criteria: \-

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Eye Institute, Affiliated Hospital of Nantong University Nantong Jiangsu

More Affiliated Hospital of Nantong University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06951087 on ClinicalTrials.gov ↗ ← All trials in China