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The Efficacy of Patients With Moderate to Severe Atopic Dermatitis Treated With Chinese Herbal Medicine

Primary Purpose

Atopic Dermatitis

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Xiao-Xian-Gui-Fu-Tang
Sponsored by
Taipei Veterans General Hospital, Taiwan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atopic Dermatitis focused on measuring Atopic Dermatits, Chinese herbal medicine, Integrative medicine

Eligibility Criteria

6 Years - 30 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 6 years old to 30 years old.
  • Diagnosis as an atopic dermatitis patient.
  • The score of the SCORAD is over 20. (moderate to severe atopic dermatitis)

Exclusion Criteria:

  • Secondary bacterial infections
  • Received oral or intravenous steroid treatment, anti-biotics, phototherapy, or other immunosuppressive therapies in the previous 2 months.
  • Received Chinese herbal medicine treatment or acupuncture.
  • Pregnant woman or current breastfeeding.
  • Who had catastrophes illness now or in the past must be avoided.
  • Can not sign informed consent or can not communicate with the researcher.
  • Abnormal liver enzymes.
  • Abnormal kidney function tests (1.5 times higher than the upper normal limit)

Sites / Locations

  • Center for Traditional Medicine, Taipei VGH
  • Taipei Veterans General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Group A

Group B

Arm Description

Group A will receive Xiao-Xian-Gui-Fu-Tang three times per day for 6 weeks, then entry 2 weeks wash-out period. Then switch to receive the placebo for another 6 weeks. Post-follow-up will be 4 weeks later.

Group B will receive a placebo three times per day for 6 weeks, then entry 2 weeks wash-out period. Then switch to receive the Xiao-Xian-Gui-Fu-Tang for another 6 weeks. Post-follow-up will be 4 weeks later.

Outcomes

Primary Outcome Measures

Changes of SCORing Atopic Dermatitis(SCORAD) Index
SCORAD is a clinical tool used to assess the extent and severity of eczema (SCORing Atopic Dermatitis). Dermatologists may use this tool before and after treatment to determine whether the treatment has been effective.
Changes of Dermatology Life Quality Index(DLQI)
The DLQI is designed to measure the health-related quality of life of adult patients suffering from a skin disease.
Changes of Children's Dermatology Life Quality Index(CDLQI)
The Children's Dermatology Life Quality Index (CDLQI) is designed to measure the impact of any skin disease on the lives of children.

Secondary Outcome Measures

Blood test (AST)
blood test at baseline, week 6, and follow-up (14 weeks)
Blood test (ALT)
blood test at baseline, week 6, and follow-up (14 weeks)
Blood test (Serum Creatinine)
blood test at baseline, week 6, and follow-up (14 weeks)
Changes of Constitution in Chinese Medicine Questionnaire
The Constitution in Chinese Medicine Questionnaire (CCMQ) consists of 60 items to classify a person into one or more of nine Body constitution(BC) types: gentleness (8 Items), Qi-deficiency (8 Items), Yang-deficiency (7 Items), Yin-deficiency (8 Items), phlegm-wetness (8 Items), wetness-heat (6 Items), blood-stasis (7 Items), Qi-depression (7 Items), and special diathesis (7 Items). Coexistence of multiple imbalanced BC types was possible which is consistent with the TCM theories. The scoring algorithm proposed in the original CCMQ was adopted in this study. A higher score in the CCMQ BC scale indicates a higher likelihood of the specific BC type, and a score of 30 is set as threshold for case definition. The CCMQ will be conducted at baseline, 12 weeks, and follow-up (16 weeks).

Full Information

First Posted
December 16, 2020
Last Updated
December 27, 2020
Sponsor
Taipei Veterans General Hospital, Taiwan
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1. Study Identification

Unique Protocol Identification Number
NCT04686955
Brief Title
The Efficacy of Patients With Moderate to Severe Atopic Dermatitis Treated With Chinese Herbal Medicine
Official Title
The Efficacy of Patients With Moderate to Severe Atopic Dermatitis Treated With Chinese Herbal Medicine
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Anticipated)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Taipei Veterans General Hospital, Taiwan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Conduct a clinical trial of integration of Chinese and Western medicine to evaluate whether the association of traditional Chinese medicine therapy has a remission effect on atopic dermatitis, and to explore the remission of lesions after an association of Chinese herbal medicine, and the correlation of syndrome differentiation types before and after treatment with Chinese and Western medicine, with a view to better understand the efficacy of atopic dermatitis in the treatment of the same disease in Traditional Chinese Medicine, and provide another option for patients with atopic dermatitis.
Detailed Description
This examination will be posted at Taipei Veterans General Hospital to recruit 24 participants who meet the inclusion criteria of atopic dermatitis to do the study. After participants agreeing to the clinical study and signing the consent form, the investigators are going to separate them into the A group (12 participants) and the B group (12 participants). The tests are going to take a total of 14 weeks. Participants need to pass the international diagnostic criteria Hannifin and Rajka to be determined as patients with atopic dermatitis. After, participants need test by scoring Atopic Dermatitis Index (SCORAD) to be determined as mild to moderate atopic dermatitis and accept the Wang Qi Traditional Chinese Medical Constitutional Scale (TCMCS), dermatological quality of life index (DLQI) score or children's skin disease quality of life index (CDLQI) score, routine blood tests, liver and kidney function tests, immunological markers associated with atopic dermatitis Diagnosis of (eosinophils count, ECP, and IgE), tongue diagnosis, and pulse diagnosis. After the collection of data is completed, the investigators will be analyzing the data by SPSS version 21 as a two-paired t-test, ANOVA statistical method, and P <0.05 as a significant result.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis
Keywords
Atopic Dermatits, Chinese herbal medicine, Integrative medicine

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
Group A will receive Xiao-Xian-Gui-Fu-Tang three times per day for 6 weeks, then entry 2 weeks wash-out period. Then switch to receive the placebo for another 6 weeks. Post-follow-up will be 4 weeks later.
Arm Title
Group B
Arm Type
Placebo Comparator
Arm Description
Group B will receive a placebo three times per day for 6 weeks, then entry 2 weeks wash-out period. Then switch to receive the Xiao-Xian-Gui-Fu-Tang for another 6 weeks. Post-follow-up will be 4 weeks later.
Intervention Type
Drug
Intervention Name(s)
Xiao-Xian-Gui-Fu-Tang
Intervention Description
The Xiao-Xian-Gui-Fu-Tang includes Xiao-Feng-San 2.0g, Dang-Gui-Yin-Zi 1.2g, Bai-Xian-Pi(Cortex Dictamni Radicis) 0.4g, and Di-Fu-Zi(Fructus Kochiae) 0.5g. The Xiao-Xian-Gui-Fu-Tang will be manufactured, packaged, and labeled by the KO DA Pharmaceutical Company (Taiwan), using good manufacturing practice standards.
Primary Outcome Measure Information:
Title
Changes of SCORing Atopic Dermatitis(SCORAD) Index
Description
SCORAD is a clinical tool used to assess the extent and severity of eczema (SCORing Atopic Dermatitis). Dermatologists may use this tool before and after treatment to determine whether the treatment has been effective.
Time Frame
week 0, 3, 6, 8, 11, 14
Title
Changes of Dermatology Life Quality Index(DLQI)
Description
The DLQI is designed to measure the health-related quality of life of adult patients suffering from a skin disease.
Time Frame
week 0, 3, 6, 8, 11, 14
Title
Changes of Children's Dermatology Life Quality Index(CDLQI)
Description
The Children's Dermatology Life Quality Index (CDLQI) is designed to measure the impact of any skin disease on the lives of children.
Time Frame
week 0, 3, 6, 8, 11, 14
Secondary Outcome Measure Information:
Title
Blood test (AST)
Description
blood test at baseline, week 6, and follow-up (14 weeks)
Time Frame
week 0, 6, 14
Title
Blood test (ALT)
Description
blood test at baseline, week 6, and follow-up (14 weeks)
Time Frame
week 0, 6, 14
Title
Blood test (Serum Creatinine)
Description
blood test at baseline, week 6, and follow-up (14 weeks)
Time Frame
week 0, 6, 14
Title
Changes of Constitution in Chinese Medicine Questionnaire
Description
The Constitution in Chinese Medicine Questionnaire (CCMQ) consists of 60 items to classify a person into one or more of nine Body constitution(BC) types: gentleness (8 Items), Qi-deficiency (8 Items), Yang-deficiency (7 Items), Yin-deficiency (8 Items), phlegm-wetness (8 Items), wetness-heat (6 Items), blood-stasis (7 Items), Qi-depression (7 Items), and special diathesis (7 Items). Coexistence of multiple imbalanced BC types was possible which is consistent with the TCM theories. The scoring algorithm proposed in the original CCMQ was adopted in this study. A higher score in the CCMQ BC scale indicates a higher likelihood of the specific BC type, and a score of 30 is set as threshold for case definition. The CCMQ will be conducted at baseline, 12 weeks, and follow-up (16 weeks).
Time Frame
week 0, 6, 14

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 6 years old to 30 years old. Diagnosis as an atopic dermatitis patient. The score of the SCORAD is over 20. (moderate to severe atopic dermatitis) Exclusion Criteria: Secondary bacterial infections Received oral or intravenous steroid treatment, anti-biotics, phototherapy, or other immunosuppressive therapies in the previous 2 months. Received Chinese herbal medicine treatment or acupuncture. Pregnant woman or current breastfeeding. Who had catastrophes illness now or in the past must be avoided. Can not sign informed consent or can not communicate with the researcher. Abnormal liver enzymes. Abnormal kidney function tests (1.5 times higher than the upper normal limit)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fang-Pey Chen, MD
Phone
886-2-28757453
Email
fpchen@vghtpe.gov.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fang-Pey Chen, MD
Organizational Affiliation
Center for Traditional Medicine, Taipei Veterans General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Traditional Medicine, Taipei VGH
City
Taipei
ZIP/Postal Code
11217
Country
Taiwan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fang-Pey Chen, MD
Phone
+886-2-2875-7453
Email
fpchen@vghtpe.gov.tw
Facility Name
Taipei Veterans General Hospital
City
Taipei
Country
Taiwan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fang-Pey Chen, MD
Phone
886-2-28757453
Email
fpchen@vghtpe.gov.tw

12. IPD Sharing Statement

Plan to Share IPD
No

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The Efficacy of Patients With Moderate to Severe Atopic Dermatitis Treated With Chinese Herbal Medicine

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