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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03489837
Other study ID # HOB-048
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date January 2017
Est. completion date October 2018

Study information

Verified date November 2018
Source Hyundai Pharm
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized, double-blind, multicenter, active-controlled phase III study to evaluate the efficacy and safety of Levotuss CR tab. in comparison with Levotuss syrup in patients with cough due to acute or chronic bronchitis


Recruitment information / eligibility

Status Completed
Enrollment 272
Est. completion date October 2018
Est. primary completion date October 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 75 Years
Eligibility Inclusion Criteria:

- moderate, severe, very severe non-productive cough patients

Exclusion Criteria:

- Patients receiving a concomitant therapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Levotuss
oral taken

Locations

Country Name City State
Korea, Republic of Included Seoul national hospital,10sites Seoul

Sponsors (1)

Lead Sponsor Collaborator
Hyundai Pharm

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cough severity check 6 hours