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The efficacy of microinvasive pars plana vitrectomy versus panretinal photocoagulation in the treatment of proliferative diabetic retinopathy with high risk characteristics

The efficacy of microinvasive pars plana vitrectomy versus panretinal photocoagulation in the treatment of proliferative diabetic retinopathy with high risk characteristics

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071263
Enrollment
Unknown
Registered
2023-05-09
Start date
2023-05-04
Completion date
Unknown
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

proliferative diabetic retinopathy (PDR) with high risk characteristics

Interventions

PRP group:panretinal photocoagulation
PRP combined with anti-VEGF therapy group:panretinal photocoagulation therapy combined with intravitreal injection of anti-neovascularization drugs
PPV group:pars plana vitrectomy
PPV combined with anti-VEGF therapy group:pars plana vitrectomy combined with intravitreal injection of anti-neovascularization drugs

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. No gender limit, patients aged over 18 years. 2. Diagnosed with type 1 or type 2 diabetes. 3. According to the rating of China's Clinical Diagnosis and Treatment Guidelines for Diabetic Retinopathy (2014 Edition), the patient's DR Condition is high-risk PDR, and the criteria are as follows: Retinal neovascularization (NVE) or papillary neovascularization (NVD) occurs when NVD > 1/4-1/3 papillary diameter (DA) or NVE > 1/2DA, or is accompanied by preretinal or vitreous hemorrhage. 4. Best corrected vision > 0.05 (34 letters). 5. No previous RPR treatment history. 6. The dioptric medium is clear, and the pupil can be fully dilated to facilitate PRP treatment and obtain clearer OCT images and fundus color photography.

Exclusion criteria

Exclusion criteria: 1. Blood pressure >180/110 mmHg (1 kPa=7.5 mmHg) and other blood pressure control is not ideal. 2. Severe heart function, liver and kidney dysfunction. 3. Patients with severe cardiovascular and cerebrovascular diseases in the past 4 months. 4. Received anti-VEGF therapy in the past 2 months. 5. History of corticosteroid treatment within the past 4 months (intravitreous). 6. Patients with severe cataract, rheogenous retinal detachment, Eales disease and optic neuropathy were excluded. 7. Other patients with glaucoma, uveitis, retinal vascular obstruction, active periocular or intraocular inflammation. 8. The study eye had significant vitreoretinal fibroangiogenesis, vitreous hemorrhage, or traction retinal detachment. 9. Study eyes with iris or anterior chamber Angle neovascularization, or neovascular glaucoma.

Design outcomes

Primary

MeasureTime frame
Best corrected vision acuity;

Secondary

MeasureTime frame
CRT thickness;Macular volume;

Countries

China

Contacts

Public ContactLiu Juping

Tianjin Medical University Eye Hospital

tydlip@126.com+86 137 5203 3227

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026