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
| Type | Name | Description |
|---|---|---|
| DRUG | HL301 300mg capsule | 2 capsules at once, 3 times a day, for 7 days |
| DRUG | Placebo | 2 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.