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The effect of modified combined surgery with wide-angle viewing systems on proliferative diabetic retinopathy

Surgical treatment of proliferative diabetic retinopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023930
Enrollment
Unknown
Registered
2019-06-19
Start date
2019-06-17
Completion date
Unknown
Last updated
2019-06-26

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

Conditions

proliferative diabetic retinopathy

Interventions

combine:anterior-posterior combined surgery
control group :anterior-posterior noncombined surgery

Sponsors

The Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: There were definite PDR patients with vitreous hemorrhage (stage 4-6 of sugar reticulum). Secondly, patients with moderate diabetic cataract had indications of cataract surgery but did not affect conventional vitrectomy. Thirdly, patients had not received whole retina laser photocoagulation and cataract surgery before vitrectomy, and had received anti-vascular endothelial growth factor (VEGF) treatment before vitrectomy. Follow-up examination should be conducted at least once after operation, and the follow-up time was more than 3 months.

Exclusion criteria

Exclusion criteria: (1) Vitreous hemorrhage and optic neuropathy caused by other diseases, such as retinitis pigmentosa, glaucomatous optic neuropathy, optic neuritis, etc. (2) history of intraocular surgery or previous treatment for vitreous hemorrhage; (3) patients in non-combined surgery group who did not undergo secondary cataract surgery for various reasons; (4) patients with acute infection of external eyes; (5) uncontrollable hyperemia; Blood pressure (systolic pressure > 180 mmHg, diastolic pressure > 110 mmHg); _history of cardiovascular and cerebrovascular accident, abnormal coagulation function or long-term use of anticoagulants, systemic multiple organ failure.

Design outcomes

Primary

MeasureTime frame
vision ability;

Secondary

MeasureTime frame
iop;Operation duration;

Countries

China

Contacts

Public ContactRonghan Wu

The Eye Hospital, School of Ophthalmology and Optometry, Wenzhou Medical University

wuronghan@126.com+86 13625772422

Outcome results

None listed

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