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Danhong Injection in the Treatment of Chronic Stable Angina

NCT01681316 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 920

Last updated 2016-10-12

No results posted yet for this study

Summary

The purpose of this study is to evaluate the effect of Danhong Injection on the relief of angina with the use of the Seattle Angina Questionnaire among patients with stable angina patients

Conditions

  • Chronic Stable Angina

Interventions

DRUG

Danhong injection

A kind of injection made from two kind of Chinese herbs: salvia miltiorrhiza and safflower

OTHER

Standard medical care

Standard medical care is in accordance with China Guideline for the diagnosis and treatment of Chronic Stable Angina (2007).

DRUG

Placebo

0.9% saline added into 250ml 0.9% saline by an independent research nurse, sealed with brown bag in order to make the investigators and patients blinded, using brown infusion tube for infusion.

Sponsors & Collaborators

  • China Food and Drug Administration

    collaborator OTHER_GOV

  • China Academy of Chinese Medical Sciences

    lead OTHER

Principal Investigators

  • Zhong Wang, Professor · Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences

  • Yun-dai Chen, Professor · Chinese PLA General Hospital(301 Hospital)

  • Yong-yan Wang, Professor · Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences

  • Xiao-xi Du, Professor · China Food and Drug Administration

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2016-10-31
Completion
2016-10-31

Countries

  • China

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01681316 on ClinicalTrials.gov