ClinicalTrials.gg
Status unknownNCT03310385Updated Mar 5, 2019

Efficacy and Safety of GHX02 in the Treatment of Acute Bronchitis

A Phase 2 interventional study of GHX02 and Placebo in Acute Bronchitis, sponsored by Daejeon University. Status unknown at 1 site in Korea, Republic of. Open to participants aged 19 Years to 75 Years. Per ClinicalTrials.gov, last updated 2019-03-05.

Sponsored by Daejeon University · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2019), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
19 Years to 75 Years
Sex
All
01

Study summary

This study is a phase 2, multicentre, dose-finding, double-blind, randomized placebo-controlled trial to evaluate the efficacy and safety of two different doses of GHX02, compared with placebo, for acute bronchitis. One-hundred and fifty patients will be included in this trial and randomly assigned to either a high-dose GHX02 group(1920mg/day), standard-dose GHX02 group(960mg/day), or control group(placebo) in a 1:1:1 allocation ratio. Patients will take one of the medications three times a day for 7 days, with 3 visiting days(screening, day0, day7). On the screening day, the Korean Standard Tool of Pattern Identification of Cough and Sputum, a diagnostic system that determines therapy in Traditional Korean Medicine, will be used to allocate patients into three groups of wind-heat, wind-cold or others.

02

Conditions studied

  • Acute Bronchitis

Browse trials for

Keywords

  • Acute Bronchitis, Herbal Medicine
03

In context

Bronchitis

156 studies on the registry are indexed under Bronchitis; 21 are open to participants now.

This study's planned enrollment of 150 is below the median of 185 across 105 interventional studies indexed under Bronchitis.

Browse Bronchitis studies →

Lead sponsor

Daejeon University is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. age 19-75 years
  2. BSS ≥ 5 points at visit2 due to acute bronchitis
  3. symptoms starting within 2 weeks before study inclusion
  4. patients who consent to participate

Exclusion criteria

Exclusion Criteria:

  1. pregnant or breast-feeding
  2. treatment with antibiotics, bronchodilators, , immune-depressants, or other clinical trial medicines during the last 4 weeks before study inclusion
  3. treatment with antitussives or expectorants during the last 7 days before study inclusion
  4. history or presence of confounding respiratory disease that may affect evaluation of the efficacy of clinical medicine (e.g. chronic bronchitis, (COPD), bronchiectasis, asthma, pneumonia, cystic fibrosis, lung cancer, or active pulmonary tuberculosis)
  5. liver or renal impairment ((ALT), aspartate aminotransferase(AST), alkaline phosphatase(ALP) ≥ 3 times the normal upper limit, or creatinine> 3.0 mg/dL at screening)
  6. history or presence of cardiovascular, renal, metabolic, haematological, neurological, psychiatric, systemic, infectious disease, or malignant tumour(except where there is no recurrence for more than 5 years after surgery)
  7. history of alcoholism or substance abuse
  8. participation in other clinical drug(medicine) trials during the last 30 days before study inclusion
  9. judged by the investigators to be inappropriate for the clinical trial.
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
150 participants (estimated)

Study arms

  • Experimental
    High-dose GHX02 group(1,920mg/day)

    4 tablets of the GHX02, three times daily for 7 days

    Drug: GHX02

  • Experimental
    Standard-dose GHX02 group(960mg/day)

    2 tablets of the GHX02 and 2 tablets of the placebo, three times daily for 7 days

    Drug: GHX02 · Drug: Placebo

  • Placebo comparator
    Placebo control

    4 tablets of the placebo, three times daily for 7 days

    Drug: Placebo

Interventions

  • DrugGHX02

    Herbal medicine originating from gualouhengryunhwan

  • DrugPlacebo

    Placebo tablets

06

What researchers measure

Primary outcomes

  1. Change in BSS(Bronchitis Severity Score)

    BSS comprises the sum of five major symptom scores for acute bronchitis: cough, sputum, dyspnea, chest pain during coughing, and rales on auscultation. Each symptom is scored on a 4-point-scale (0=absent, 1=mild, 2=moderate, 3=severe, 4=very severe), with a maximum total score of 20 points. The investigator assesses symptom scores on the basis of the patient's subjective symptoms.

    Time frame: Day0, Day7

Secondary outcomes

  1. Change in Questionnaire of Clinical Symptoms of Cough and Sputum

    Questionnaire items are as follows: (1) cough -frequency, intensity, sensitivity; (2) sputum -frequency, volume, difficulty to cough-up, appearance, color; (3) activities of daily living; (4) night-time sleeping. Each item is scored on a 4-point-scale, with a total maximum score of 40 points.

    Time frame: Day0, Day7

  2. Change in Leicester Cough Questionnaire-acute(LCQ-acute)

    It consists of 19 items divided into three parts, physical, psychological, and social, each scored from 1 to 7. The total score is the sum of the average scores(1-7 points) for each part. The higher the score, the better the quality of life.

    Time frame: Day0, Day7

  3. Change in frequency of coughing fits

    participants will be classified into one of the following scales: 0 = 0 time/day, 1 = 1 time/day, 2 = 2-3 times/day, 3 = 4-5 times/day(sometimes), 4 = 6-10 times/day(frequent), 5 = over 15 times/day(consistently).

    Time frame: Day0, Day1, Day2, Day3, Day4, Day5, Day6, Day7

  4. Integrative Medicine Outcome Scale(IMOS)

    It's a 5-point-scale for evaluating improvement after treatment (where, 1=complete recovery, 2=major improvement, 3=slight-to-moderate improvement, 4=no change, 5=deterioration), either by the patient or investigator (the investigator in this trial).

    Time frame: Day7

  5. Integrative Medicine Patient Satisfaction Scale(IMPSS)

    It's a 5-point-scale for evaluating patient satisfaction with the treatment (where, 1=very satisfied, 2=satisfied, 3=neutral, 4=dissatisfied, 5=very dissatisfied)

    Time frame: Day7

07

Study locations

1 site
  • Dunsan Korean Medicine Hospital, Daejeon University
    Daejeon, Korea, Republic of
    • Yee Ran Lyu · Contact
08

References and documents

Publications

  • Ji KY, Kim KM, Oh JJ, Kim JW, Lee WJ, Cho H, Lee HK, Lee JY, Chae S. Assessment of the 4-week repeated-dose oral toxicity and genotoxicity of GHX02. J Appl Toxicol. 2020 Feb;40(2):270-284. doi: 10.1002/jat.3902. Epub 2019 Sep 12. PubMed 31515828 ↗
  • Lyu YR, Yang WK, Park SJ, Kim SH, Kang WC, Jung IC, Park YC. Efficacy and safety of GHX02 in the treatment of acute bronchitis: protocol of a phase II, double-blind, randomised placebo-controlled trial. BMJ Open. 2018 May 14;8(5):e019897. doi: 10.1136/bmjopen-2017-019897. PubMed 29764875 ↗

Individual participant data

Plan to share: Yes

Supporting information: Study protocol

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03310385
Lead sponsor
Daejeon University
Responsible party
Yang Chun Park (Professor, Daejeon University) — Principal investigator
First posted
Oct 16, 2017
Start date
Mar 18, 2019 (estimated)
Primary completion
Mar 2020 (estimated)
Completion
Mar 2020 (estimated)
Last update
Mar 5, 2019

Study contacts

YeeRan Lyu
Contact
yyr900511@gmail.com
82424709663

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion