Clinical Trials Directory

Trials / Completed

CompletedNCT02250027

A Multicenter, Randomized, Double-blind, Parallel Group Study to Determine the Optimal Dose of HL301 After 7 Days Oral Administration in Acute Bronchitis or Acute Exacerbations of Chronic Bronchitis Patients (HL301: Mixed Extract of Rehmannia Glutinosa, Schisandra and so on)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
156 (actual)
Sponsor
Hanlim Pharm. Co., Ltd. · Industry
Sex
All
Age
19 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the optimal dose of HL301 in patients with acute bronchitis or acute exacerbations of chronic bronchitis. \- BSS(Bronchitis Severity Score), BCSS(Breathlessness, Cough, and Sputum Scale), evaluation of symptoms of cough and sputum

Conditions

Interventions

TypeNameDescription
DRUGHL301 300mg capsule2 capsules at once, 3 times a day, for 7 days
DRUGPlacebo2 capsules at once, 3 times a day, for 7 days

Timeline

Start date
2014-03-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2014-09-26
Last updated
2014-09-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02250027. Inclusion in this directory is not an endorsement.