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Chinese Herbal Medicine Formula Combined With Inhaled Corticosteroids for the Treatment of Mild to Persistent Asthma in Children

Primary Purpose

Childhood Asthma

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang)
10% CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang)
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Childhood Asthma focused on measuring childhood asthma, inhaled corticosteroids, Chinese medicine, Ma-Hsing-Kan-Shih-Tang, Liu-Jun-Zi-Tang

Eligibility Criteria

4 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged 4-11 years old
  • GINA (Global Initiative for Asthma) guideline belong to mild to moderate asthmatic children
  • regular use low dose ICS+ LABA or medium dose ICS at least one month

Exclusion Criteria:

  • asthma with acute exacerbation or ever has used systemic steroids in recent one month
  • psychiatric disease or behavior disorder
  • ever has received Chinese herbal medicine or other traditional Chinese medicine treatment in recent two weeks

Sites / Locations

  • China Medical University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

CM group

placebo group

Arm Description

Outcomes

Primary Outcome Measures

The change of Childhood Asthma Control Test (cACT)
cACT questionnaire is a tool to evaluate asthma symptoms

Secondary Outcome Measures

The change of FEV1/FVC (%) in spirometry
Spirometry can be used to easily evaluate pulmonary function for children older than 6 years old. Participants who are unable to perform forced expiratory maneuvers will use Impulse Oscillometry System (IOS) instead.
The change of CBC/DC
Blood test includes , total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of total IgE
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of the ECP
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of IL-4
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of IL-5
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of IL-13
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
The change of scores of the Integrated Therapeutics Group Child Asthma Short Form (ITG-CASF)
ITG-CASF is a tool to measure symptoms and disability in pediatric asthma patients
The change of scores of Pediatric Asthma Caregiver's Quality of Life Questionnaire (PACQLQ)
PACQLQ is designed to measure the limitations and anxieties faced by caregivers of children with asthma.

Full Information

First Posted
September 7, 2021
Last Updated
October 1, 2021
Sponsor
China Medical University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05066841
Brief Title
Chinese Herbal Medicine Formula Combined With Inhaled Corticosteroids for the Treatment of Mild to Persistent Asthma in Children
Official Title
Chinese Herbal Medicine Formula Combined With Inhaled Corticosteroids for the Treatment of Mild to Persistent Asthma in Children: a Randomized Double-blind Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 25, 2021 (Anticipated)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
China Medical University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of study is to provide an objective data for evaluating the efficacy and safety of Chinese medicine (CM) formula combined with inhaled corticosteroid in the treatment of asthmatic children. Investigators will recruit eighty-six mild to moderate asthmatic children aged 4-11 years old with regular ICS usage and they will be randomized into two groups in this double-blind trial. Forty-three subjects will receive CM (CM group; Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang) and the other forty-three subjects will receive placebo (placebo group; 10% CM) for 12 weeks. Investigators will compare these two groups by questionnaires of Childhood Asthma Control Test (cACT), the Integrated Therapeutics Group Child Asthma Short Form (ITG-CASF), Pediatric Asthma Caregiver's Quality of Life Questionnaire (PACQLQ), the pulmonary function test and blood test including Complete Blood Count with Differential Count (CBC/DC), total IgE, Eosinophil Cationic Protein (ECP) and IL-4/IL-5/IL-13. Adverse events, renal and liver function test will be evaluated to investigate the safety of CM formula as well.
Detailed Description
Treating pediatric asthma has been in accordance with GINA guidelines by stepwise approach to adjust treatment for individual patient needs. However, most of the asthma controller medication nowadays is inhaled corticosteroids (ICS). Parents with steroid phobia may raise concern and fears about the potential systemic effects, leading to poor adherence to medication and worse control. This study aims to evaluate the efficacy and safety of Chinese medicine (CM) formula combined with inhaled corticosteroid for the treatment of mild to moderate persistent asthma in children. Investigators focus on the following specific aims: Aim 1. To determine the efficacy of the CM formula (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang) compared with placebo; Aim 2. To evaluate the effects of CM formula on quality of life in these patients with pediatric asthma; Aim 3. To investigate the safety of CM formula in these patients with pediatric asthma. Eighty-six mild to moderate asthmatic children aged 4-11 years old with regular ICS usage will be randomized into two groups in this double-blind trial. Forty-three subjects will receive CM (CM group; Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang) and the other forty-three subjects will receive placebo (placebo group; 10% CM) for 12 weeks. The evaluation including pulmonary function test, IOS, FeNO, blood test, questionnaire and asthma diary card of both two groups will be conducted during the study period. The safety of CM formula use will be investigated by recording the adverse events and renal and liver function test as well. This study will provide an objective data for evaluating the efficacy and safety o of Chinese medicine (CM) formula combined with inhaled corticosteroid in the treatment of asthmatic children. Through the combination of Chinese and western medicine, we expect to enhance the efficacy of asthma treatment, reduce acute exacerbation and tapper the dose of inhaled corticosteroids, leading to better quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Asthma
Keywords
childhood asthma, inhaled corticosteroids, Chinese medicine, Ma-Hsing-Kan-Shih-Tang, Liu-Jun-Zi-Tang

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
86 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CM group
Arm Type
Experimental
Arm Title
placebo group
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang)
Intervention Description
CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang) for 12 weeks
Intervention Type
Drug
Intervention Name(s)
10% CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang)
Intervention Description
10% CM (Ma-Hsing-Kan-Shih-Tang in combination with Liu-Jun-Zi-Tang) and 90% starch for 12 weeks
Primary Outcome Measure Information:
Title
The change of Childhood Asthma Control Test (cACT)
Description
cACT questionnaire is a tool to evaluate asthma symptoms
Time Frame
week 12
Secondary Outcome Measure Information:
Title
The change of FEV1/FVC (%) in spirometry
Description
Spirometry can be used to easily evaluate pulmonary function for children older than 6 years old. Participants who are unable to perform forced expiratory maneuvers will use Impulse Oscillometry System (IOS) instead.
Time Frame
week 12
Title
The change of CBC/DC
Description
Blood test includes , total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of total IgE
Description
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of the ECP
Description
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of IL-4
Description
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of IL-5
Description
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of IL-13
Description
Blood test includes CBC/DC, total IgE, ECP and cytokines (IL-4/IL-5/IL-13) to evaluate the immunological function.
Time Frame
week 12
Title
The change of scores of the Integrated Therapeutics Group Child Asthma Short Form (ITG-CASF)
Description
ITG-CASF is a tool to measure symptoms and disability in pediatric asthma patients
Time Frame
week 12
Title
The change of scores of Pediatric Asthma Caregiver's Quality of Life Questionnaire (PACQLQ)
Description
PACQLQ is designed to measure the limitations and anxieties faced by caregivers of children with asthma.
Time Frame
week 12
Other Pre-specified Outcome Measures:
Title
The frequency of acute exacerbation
Description
The frequency of acute exacerbation such as ER visit and admission will be recorded in asthma diary.
Time Frame
week 12
Title
Adverse drug reaction (ADR) during study period
Description
ADR during study period will be recorded in asthma diary.
Time Frame
week 12
Title
The change of the renal function test
Description
Renal function test including BUN and Creatinine will to evaluate the safety of CM usage
Time Frame
week 12
Title
The change of the liver function test
Description
Liver function test including AST and ALT will to evaluate the safety of CM usage
Time Frame
week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: aged 4-11 years old GINA (Global Initiative for Asthma) guideline belong to mild to moderate asthmatic children regular use low dose ICS+ LABA or medium dose ICS at least one month Exclusion Criteria: asthma with acute exacerbation or ever has used systemic steroids in recent one month psychiatric disease or behavior disorder ever has received Chinese herbal medicine or other traditional Chinese medicine treatment in recent two weeks
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chieh Wang
Phone
+886963619537
Email
u9923035@cmu.edu.tw
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
ZIP/Postal Code
404
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chieh Wang
Phone
+886963619537
Email
u9923035@cmu.edu.tw

12. IPD Sharing Statement

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Chinese Herbal Medicine Formula Combined With Inhaled Corticosteroids for the Treatment of Mild to Persistent Asthma in Children

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