A Clinical Evaluation of Baofeikang Granule in Combined Pulmonary Fibrosis and Emphysema Treatment

NCT02805699 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2017-08-30

No results posted yet for this study

Summary

The purpose of this study is to confirm the efficacy and safety of BaofeiKang Granule in the treatment of Combined Pulmonary Fibrosis and Emphysema patients.

Conditions

  • Combined Pulmonary Fibrosis and Emphysema

Interventions

DRUG

Baofeikang Granule

To observe the efficacy and safety of Baofeikang granules on Combined Pulmonary Fibrosis and Emphysema Treatment.Baofeikang Granules consist of(Codonopsis 30g, Cordyceps fungi powder 12g, ophiopogon root 10g, Schisandra 10g, angelica 15g, Bulbus Fritillariae thunbergii 10g, Sophora flavescens 10g,Forsythia suspensa 12g,Pinellia 10g, saponins thorn 10g, Radix Peucedani 10g).1 bags,P.O(Oral)twice of each 3 months cycle.

DRUG

Placebo

On the basis of comprehensive treatment of spasmolysis antiasthmatic and anti-inflammatory, expectorant, cough , give Chinese medicine placebo,1 bags,P.O(Oral)twice of each 3 months cycle.

Sponsors & Collaborators

  • Beijing Municipal Science & Technology Commission

    lead OTHER

Principal Investigators

  • hongsheng cui, Ph.D,Professor · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • weibo Bi, Master · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • jianjun Wu, Master · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • ruifeng Jin, Master · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • chang'an Li, Master · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • minmin Shan, Master · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • qiuyi Chen, Bachelor · The Third Affiliated Hospital of Beijing University of Chinese Medicine

  • shengtao li, Bachelor · The Third Affiliated Hospital of Beijing University of Chinese Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2019-06-30
Completion
2019-09-30

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 NCT02805699 on ClinicalTrials.gov