drugset / Trial / NCT03258242

A Study of Keluo Xin Capsule Compare to Placebo in Terms of Efficacy and Safety in Patients With Diabetic Retinopathy

NCT03258242 ↗

Phase 2 Unknown 198 enrolled Chengdu Kanghong Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a study aiming to assess the efficacy and safety of Keluo Xin capsule in patients with moderately severe to severe nonproliferative diabetic retinopathy (NPDR). Two-thirds of participates will receive Keluo Xin capsules while other one third will receive placebo.

Timeline

Start
2017-08-31
Primary completion
2019-08-31
Completion
2020-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Keluo Xin Unknown 4 unknown Oral