Anti-VEGF in Real-world

NCT ID: NCT05222633

Last Updated: 2022-02-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-01-01

Study Completion Date

2023-05-01

Brief Summary

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Anti-vascular endothelial growth factor therapy is the major intervention for treating ischemic retina diseases. According to FDA and China Food and Drug Administration, Ranibizumab, Aflibercept, and Conbercept are major types of anti-vascular endothelial growth factor therapy drugs. In the current study, the primary aim is to observe the visual acuity, anatomy effect of anti-vascular endothelial growth factor therapy in the real-world setting.

Detailed Description

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Anti-vascular endothelial growth factor therapy is the major intervention for treating ischemic retina diseases, including neovascular age-related macular edema, diabetic macula edema/non-proliferative diabetic retinopathy / proliferative diabetic retinopathy, retinal vein occlusions related macular edema, and choroidal neovascularization secondary to multiple retinal diseases. According to FDA and China Food and Drug Administration, Ranibizumab, Aflibercept, and Conbercept are major types of anti-VEGF drugs. In the current study, the primary aim is to aim to observe the visual acuity, anatomy effect of anti-vascular endothelial growth factor therapy in the real-world setting.

Conditions

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Neovascular Age-related Macular Edema Diabetic Macular Edema Choroidal Neovascular Membrane Non-proliferative Diabetic Retinopathy Retinal Vein Occlusion Proliferative Diabetic Retinopathy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Neovascular age-related macular edema

Patients with new-onset and recurrent Neovascular age-related macular edema.

Ranibizumab

Intervention Type DRUG

Ranibizumab 0.5mg/0.05ml intravitreal injection

Aflibercept

Intervention Type DRUG

Aflibercept 2.0mg/0.05ml intravitreal injection

Conbercept

Intervention Type DRUG

Conbercept 0.5mg/0.05ml intravitreal injection

Diabetic macula edema

Patients with new-onset and recurrent diabetic macula edema

Ranibizumab

Intervention Type DRUG

Ranibizumab 0.5mg/0.05ml intravitreal injection

Aflibercept

Intervention Type DRUG

Aflibercept 2.0mg/0.05ml intravitreal injection

Conbercept

Intervention Type DRUG

Conbercept 0.5mg/0.05ml intravitreal injection

Non-proliferative diabetic retinopathy/proliferative diabetic retinopathy

Patients with new-onset and recurrent non-proliferative diabetic retinopathy/proliferative diabetic retinopathy

Ranibizumab

Intervention Type DRUG

Ranibizumab 0.5mg/0.05ml intravitreal injection

Aflibercept

Intervention Type DRUG

Aflibercept 2.0mg/0.05ml intravitreal injection

Conbercept

Intervention Type DRUG

Conbercept 0.5mg/0.05ml intravitreal injection

Retinal vein occlusions

Patients with new-onset and recurrent retinal vein occlusions

Ranibizumab

Intervention Type DRUG

Ranibizumab 0.5mg/0.05ml intravitreal injection

Choroidal neovascularization

Patients with new-onset and recurrent choroidal neovascularization

Ranibizumab

Intervention Type DRUG

Ranibizumab 0.5mg/0.05ml intravitreal injection

Aflibercept

Intervention Type DRUG

Aflibercept 2.0mg/0.05ml intravitreal injection

Conbercept

Intervention Type DRUG

Conbercept 0.5mg/0.05ml intravitreal injection

Interventions

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Ranibizumab

Ranibizumab 0.5mg/0.05ml intravitreal injection

Intervention Type DRUG

Aflibercept

Aflibercept 2.0mg/0.05ml intravitreal injection

Intervention Type DRUG

Conbercept

Conbercept 0.5mg/0.05ml intravitreal injection

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients with neovascular age-related macular edema (nAMD), diabetic macula edema (DME)/non-proliferative diabetic retinopathy (NPDR)/ proliferative diabetic retinopathy (PDR), retinal vein occlusions related macular edema, and choroidal neovascular (CNV) secondary to multiple retinal diseases.
* Undergo intravitreal anti-VEGF therapy

Exclusion Criteria

* unable to receive OCT examination
* Severe corneal opacity, cataract that affect OCT examination
Minimum Eligible Age

35 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Wenbin Wei

OTHER

Sponsor Role lead

Responsible Party

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Wenbin Wei

Director

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Wenbin Wei, MD

Role: STUDY_DIRECTOR

Beijing Tongren Hospital

Locations

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Wen-Bin Wei

Beijing, Beijing Municipality, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Wenbin Wei, MD

Role: CONTACT

010-58269523

Facility Contacts

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Wen-Bin Wei, MD

Role: primary

Other Identifiers

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Anti-VEGF in real-world

Identifier Type: -

Identifier Source: org_study_id

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