Viewing Study NCT02769169


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Study NCT ID: NCT02769169
Status: TERMINATED
Last Update Posted: 2019-09-19
First Post: 2016-05-01
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Double-dose Ranibizumab for Polypoidal Choroidal Vasculopathy
Sponsor: Sun Yat-sen University
Organization:

Study Overview

Official Title: Double-dose Ranibizumab for Polypoidal Choroidal Vasculopathy: A Prospective Randomized Multicenter Study
Status: TERMINATED
Status Verified Date: 2019-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: study protocol changed
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether double-dose Ranibizumab are effective to regress the polyps and benefit to the visual outcome in the polypoidal choroidal vasculopathy (PCV).
Detailed Description: Recently, it's reported that intravitreal high dose Lucentis®(Ranibizumab) could benefit to both regression of the polyps and the relief of macular edema in PCV patients. Since it was a single arm prospective study with a relatively small sample size, randomized clinical trials were needed to confirm the efficacy of high dose Ranibizumab in PCV treatment. In this study, the investigator will compare the efficacy of double-dose (1mg, 3+prn) Raibizumab with regular dose (0.5mg, 3+prn) for PCV treatment.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: