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Clinical Trial Summary

This is a post-marketing drug safety monitoring study in a prospective manner, and data collection will be performed in a registration-follow-up manner. Safety information about patients who have received intravitreal injection of Conbercept Ophthalmic Injection in medical institutions involved in the study during research will be actively monitored without intervening in diagnosis and treatment. All patients enrolled will be followed up for one year.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03054818
Study type Observational
Source Chengdu Kanghong Biotech Co.,Ltd.
Contact Ningli Wang
Phone 010-58265922
Email wningli@vip.163.com
Status Recruiting
Phase N/A
Start date October 2016
Completion date June 2018