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Intravitreal Ranibizumab Injection as Adjuvant in the Treatment of Postvitrectomy Diabetic Vitreous Hemorrhage Accompanied by Neovascular Glaucoma

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02647515
Enrollment
18
Registered
2016-01-06
Start date
2013-01-31
Completion date
2014-12-31
Last updated
2016-01-06

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

Conditions

Diabetic Retinopathy, Glaucoma, Neovascular

Brief summary

To determine the efficacy of intravitreal ranibizumab injection as adjuvant therapy in the treatment of postvitrectomy diabetic vitreous hemorrhage (PDVH) accompanied by neovascular glaucoma (NVG) as a means of preventing recurrent vitreous hemorrhage (VH) and optimizing postoperative intraocular pressure(IOP)control.

Interventions

DRUGranibizumab

Sponsors

Ningbo University
CollaboratorOTHER
Ruijin Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age≥18 years * PDVH obscuring the disc and vessels for more than 14 days and no evidence of retinal detachment after primary vitrectomy for PDR-related complications such as nonclearing VH, macula-involving or macula-threatening tractional retinal detachment, or fibrovascular proliferation with vitreoretinal adhesions * NVG occurred following PDVH less than 4 weeks (NVG was diagnosed when an IOP elevation of 22mmHg or more was accompanied by neovascularization of the iris and/or the anterior chamber angle)

Exclusion criteria

* intraoperative use of long-acting gas or silicone oil in primary vitrectomy, repeat vitrectomy after primary vitrectomy for retinal diseases other than VH, previous history of vitrectomy * previous intravitreal injection of ranibizumab or bevacizumab in either eye * previous intravitreal corticosteroids injection in either eye * pregnancy or current oral contraceptive intake * usage of clopidogrel bisulfate or coumadin * uncontrolled hypertension and cardiac disease * uncontrolled renal or liver disease

Design outcomes

Primary

MeasureTime frame
vitreous hemorrhage12 months
intraocular pressure12 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026