Skip to main content
OpenTrials
Completed

NCT Number: NCT04089605

Ranibizumab vs Dexamethasone Implant in Vitrectomized Eyes With Diabetic Macular Edema

Vitrectomy is required for removal of vitreous hemorrhage or retinal traction tissue in some patients with proliferative diabetic retinopathy. Post-vitrectomy macular edema may occur in these diabetic patients. Intravitreal injections of anti-VEGF agents or corticosteroid are required for treating diabetic macular edema (DME) in vitrectomized eyes. Intraocular levels of various cytokines may alter in the diabetic eyes following vitrectomy. Pharmacokinetics may be different between various intraocular agents in vitrectomized eyes. Herein our study will prospectively randomize to compare the clinical behavior between intravitreal ranibizumab (IVR) and intravitreal dexamethasone implant (IDI) in vitrectomized patients with DME. To our knowledge, it is the first study involving such subject.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Far Eastern Memorial Hospital

New Taipei City, 105, Taiwan

About this study

Vitrectomy is required for removal of vitreous hemorrhage or retinal traction tissue in some patients with proliferative diabetic retinopathy. Post-vitrectomy macular edema may occur in these diabetic patients. Intravitreal injections of anti-VEGF agents or corticosteroid are required for treating diabetic macular edema (DME) in vitrectomized eyes. Intraocular levels of various cytokines may alter in the diabetic eyes following vitrectomy. Pharmacokinetics may be different between various intraocular agents in vitrectomized eyes. Herein our study will prospectively randomize to compare the clinical behavior between intravitreal ranibizumab (IVR) and intravitreal dexamethasone implant (IDI) in vitrectomized patients with DME. To our knowledge, it is the first study involving such subject.

Pseudophakic vitrectomized eyes with treatment-naïve center-involved DME will be enrolled with one eye in each patient. They are randomized into one group receiving IDI every 3 to 4 months, and the other group undergoing IVR using 3 monthly plus treat-and-extend injections all with monthly follow-up for 6 months. Switch of intravitreal drugs or deferred macular laser is not allowed. Primary outcome measures include change in central foveal thickness (CFT) in 1 mm by spectral-domain optic coherence tomography, and best corrected visual acuity (BCVA) at Month 6. Primary outcome measures include change in CFT and BCVA at Month 6. Injection number, BCVA, CFT, post-injection complications, and IOP are recorded and compared with Wilcoxon signed rank test within the group and Wilcoxon rank sum test between groups. Fisher's exact test is used for categorical comparison between groups. P value less than 0.05 is considered significant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age more than 18 years
  • Glycosylated hemoglobin (HbA1c) less than 10.0%
  • Best-corrected visual acuity (BCVA) between 20/400 to 20/40
  • Central foveal thickness (CFT) more than 300 μm in the 1-mm central macular subfield on spectral domain optical coherence tomography (SD-OCT, CIRRUS™ HD-OCT 5000, Carl Zeiss Meditec Inc., Dublin, CA, USA) using 6 radial line scans through the fovea
  • Macular leakage on fundus fluorescein angiography (HRA2, Heidelberg Engineering GmbH, Germany)
  • The DME pattern can include submacular fluid, cystoid change, and diffuse macular thickening
  • All have proliferative diabetic retinopathy treated by panretinal photocoagulation receiving prior vitrectomy without silicone oil or gas inside the vitreous cavity
  • Prior intraocular surgery performed as least 3 months ago

Exclusion criteria

  • Pregnant or nursing women
  • The patients with the history of thromboembolic events or major surgery within the previous 3 months
  • Presence of anterior chamber intraocular lens or subluxated/dislocated posterior chamber intraocular lens
  • Presence of uncontrolled hypertension
  • Known coagulation abnormalities or current use of anticoagulative medication other than aspirin
  • Prior macular photocoagulation or photodynamic therapy
  • Presence of active infectious disease or intraocular inflammation
  • Intraocular pressure more than 20 mmHg or glaucoma history
  • Presence of iris neovascularization/vitreous hemorrhage.
  • The DME pattern with accompanying macular traction by epiretinal membrane or posterior hyaloid

Treatment and study plan

Dexamethasone implant

Drug

intravitreal dexamethasone implant injections in vitrectomized patients with DME

Other names: Dexamethasone implants (Ozurdex®, Allergan Inc., Irvine, CA, USA)

ranibizumab

Drug

intravitreal ranibizumab injections in vitrectomized patients with DME

Other names: (Lucentis®, Ranibizumab (Novartis Pharma AG, Basel, Switzerland, and Genentech Inc., South San Francisco, CA, USA)

Primary outcomes

  1. BCVA at Month 6

    Time frame: Month 6

    best-corrected visual acuity (BCVA) at the end of intervention

  2. CFT at Month 6

    Time frame: Month 6

    central foveal thickness (CFT) at the end of intervention

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Official study title

Ranibizumab and Dexamethasone Implant in Vitrectomized Eyes With Diabetic Macular Edema

Important dates

Study start
2017
Primary completion
2018
Study completion
2019
First posted
Sep 13, 2019
Registry last updated
Sep 13, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.