Early Laser Treatment for Diabetic Eye Disease in China : A Pilot Randomized Trial

Last updated: May 6, 2022
Sponsor: Sun Yat-sen University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Diabetic Retinopathy

Retina

Treatment

N/A

Clinical Study ID

NCT02956759
ZOC-PEARL STUDY
  • Ages 18-80
  • All Genders

Study Summary

To compare immediate laser pan-retinal photocoagulation (PRP) treatment of severe or very severe non proliferative diabetic retinopathy (NPDR) stage versus deferral of treatment until the appearance of any proliferative diabetic retinopathy (PDR) in rural and urban patients in China.

Interview data from some patients and survey data from ophthalmologists in the study hospitals will help determine acceptability of early treatment, and how to overcome barriers to increased use of this option.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adults aged >= 18 years with untreated DR at severe or very severe NPDR stage ineither one or both eyes, according to the clinical opinion of the investigator.
  • Sufficiently clear ocular media to allow visualization of the retina and retinalphotography in either eye.
  • Capable of giving informed consent.

Exclusion

Exclusion Criteria:

  • DR at later stage of retinopathy than severe or very severe (eg, two or more of the 4-2-1 criteria are met) NPDR in either eye, but a patient may be enrolled if one eyehas severe or very severe NPDR and the fellow eye has PRP-treated PDR and has beenstable after treatment.
  • Clinically significant macular edema in either eye.
  • Dense cataracts or other media opacity preventing visualization of the retina in theeye.
  • History of previous surgical or laser treatment for DR or other retinal conditions ina study eye, including history of anti-VEGF or corticosteroid injection or focal laserfor DME within 6 months, or any history of scleral buckle, vitrectomy or other retinaldetachment repair.
  • History of other retinal vascular disorders including CRVO, CRAO, BRVO, BRAO in thestudy eye.
  • Previous cataract or glaucoma surgery is specifically allowed if performed ≥ 6 weeksprior to enrollment.
  • Pregnancy.
  • Severe renal insufficiency treated with hemodialysis treatment, kidney transplant,pancreatic transplant, and intensive insulin therapy initiated within 4 months.
  • Nystagmus, unable to cooperate with laser treatment.

Study Design

Total Participants: 200
Study Start date:
October 01, 2016
Estimated Completion Date:
October 31, 2023

Study Description

China now has the world's largest number of diabetic persons. Population studies show that only 10% of Chinese rural-dwellers with DR receive therapy. The current standard approach to treatment of DR often requires patients to return for multiple examinations over years, before they reach trial-proven criteria for treatment. This long process is ill-suited to support good compliance with care in low-resource settings. Our recent published review suggests that earlier PRP treatment, which could reduce the burden of compliance, may be clinically effective and cost effective, but the current evidence base is insufficient to make a firm recommendation.

Connect with a study center

  • Zhongshan Ophthalmic Center

    Guangzhou, Guangdong 510000
    China

    Active - Recruiting

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