Comparing Conventional Grid Laser Photocoagulation and Subthreshold Micropulse Laser in Diabetic Macular Edema Using OCT Angiography
Launched by CHINESE UNIVERSITY OF HONG KONG · Jun 8, 2022
Trial Information
Current as of June 13, 2025
Unknown status
Keywords
ClinConnect Summary
Laser photocoagulation was previously a mainstay treatment for DME before the introduction of anti-vascular endothelial growth factor (anti-VEGF) agents injection. Vascular endothelial growth factor (VEGF) is an important mediator of blood-retinal barrier breakdown, which leads to fluid leakage and the development of macular edema \[5\]. Observing that intraocular VEGF levels are increased in DME, using VEGF inhibitors (anti-VEGF) was found to be beneficial in reversing vision loss from macular edema \[6\]. In recent years, many large-scale studies \[7\], \[8\], \[9\], \[10\] had proven tha...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with best-corrected visual acuity better than 20/200 (checked with refraction test)
- • Patients with clinically significant diabetic macular edema (DME) who have not received any treatment within 6 months
- • Patients with central retinal thickness equal / above to around 400 um
- • Patients who are able to have regular visits after laser treatment for at least 6 months
- Exclusion Criteria:
- • Children under the age of 18
- • Patients with proliferative diabetic retinopathy
- • Patients with co-existing retinal or macular disease, including epiretinal membrane and vitreomacular traction
- • Patients with previous history of laser photocoagulation, anti-VEGF injection, intravitreal steroid injection, vitreoretinal or cataract surgery within a period of 6 months
- • Patients with history of uveitis
- • Patients who are unfit or for capturing of OCT-A images
- • Patients with significant media opacity that may interfere with fundal examination and the acquisition of high quality OCT-A images
- • Patients who are unable to give informed consent to enter the study
- • uncooperative
About Chinese University Of Hong Kong
The Chinese University of Hong Kong (CUHK) is a prestigious research institution renowned for its commitment to advancing medical science and improving healthcare outcomes. As a clinical trial sponsor, CUHK leverages its extensive academic resources and interdisciplinary expertise to conduct innovative research that addresses critical health challenges. The university fosters collaboration among leading researchers, healthcare professionals, and industry partners, ensuring rigorous study design and implementation. CUHK is dedicated to upholding the highest ethical standards in clinical research, with a focus on translating findings into tangible benefits for patients and the broader community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Hong Kong, , China
Patients applied
Trial Officials
Gabriel HK Li, M.B. Ch.B
Principal Investigator
CUHK
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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