The Association Between Human Microbiome and Vitamin D in Chronic Urticaria
Primary Purpose
Urticaria
Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Vitamin D
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Urticaria focused on measuring Vitamin D, human microbiome, vitamin D receptors and vitamin D binding protein
Eligibility Criteria
Inclusion Criteria:
- Experimental group: patients with chronic spontaneous urticaria under the age of 18 .
- Control group: healthy children under the age of 18 (eg, healthy siblings of sick children).
Exclusion Criteria:
- Recruit patients who have used antibiotics, systemic steroids, and immunosuppressants in the previous month.
- Patients with C1 esterase inhibitor deficiency, lymphocytopenia, thrombocytopenia, severe diseases involving heart, liver, or kidney, metabolic disease, or autoimmune disease.
Sites / Locations
- China Medical University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Treatment group
Control group
Arm Description
Vitamin D (2000IU/day) for 6 months
placebo
Outcomes
Primary Outcome Measures
Levels of vitamin D
Vitamin D will be measured in a blood sample by ELISA to determine baseline status.
Levels of vitamin D
Vitamin D will be measured in a blood sample to follow the change from baseline in vitamin D level at month 6.
Single nucleotide polymorphism of vitamin D receptor and vitamin D binding protein.
Single nucleotide polymorphism (SNP) genotyping will be performed in a blood sample by using TaqMan SNP genotyping assays.
Microbiome Microbiome
Nasal and anal swabs will be used to detect respiratory and intestinal microbiome by using 16S rRNA sequencing to determine baseline status.
Microbiome Microbiome
Nasal and anal swabs will be used to detect respiratory and intestinal microbiome by using 16S rRNA sequencing,and to follow the change from baseline in microbiome at month 6.
Total IgE
Plasma total IgE concentration will be measured by microparticle immunoassay (IMx analyzer, Abbott Laboratories, Abbott Park, IL) and ELISA to determine baseline status.
Total IgE
Plasma total IgE concentration will be measured by microparticle immunoassay (IMx analyzer, Abbott Laboratories, Abbott Park, IL) and ELISA to follow the change from baseline in total IgE at month 6.
Allergen-specific IgE
Plasma allergen-specific IgE will be measured by BioIC ®.
Secondary Outcome Measures
Quality of Life Assessment
Patients will rate their CU symptoms and the impact of their CU on various aspects of their lives. Each question is scored from 0 (not at all) to 3 (very much). Overall score, on scale of 0 to 57.
The Urticaria Activity Score 7 (UAS7)
The Urticaria Activity Score 7 measures number the weekly average of hives and pruritus measured twice a day. It scores from 0 to 42.
Full Information
NCT ID
NCT05497596
First Posted
July 11, 2022
Last Updated
September 5, 2023
Sponsor
China Medical University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05497596
Brief Title
The Association Between Human Microbiome and Vitamin D in Chronic Urticaria
Official Title
The Association Between Human Microbiome and Vitamin D in Chronic Urticaria
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 2, 2022 (Actual)
Primary Completion Date
March 31, 2025 (Anticipated)
Study Completion Date
March 31, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
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
A double-blind study to evaluate the role of human microbiome and vitamin D in the development of urticaria.
Detailed Description
Urticaria is a chronic allergic inflammatory disorder. Genetic and environmental factors, such as exposure to allergens and microbes, have a detrimental role in the development of chronic urticaria. Vitamin D also has an important role in urticaria. Lower sera vitamin D level was observed in patients that developed urticaria. Vitamin D binding protein (DBP) bound to vitamin D and regulated its metabolites in the circulation. Moreover, vitamin D receptors (VDR) have been identified on nearly all cells of the immune system. It may contribute to maintenance of intestinal barrier function by preventing increased intestinal permeability, dysbiosis, inflammation, and a lack of immune tolerance in the gut.
The investigators plan to design a double-blind trial to evaluate the role of human microbiome and vitamin D in the development of urticaria. We will enroll children with chronic urticaria (CU) and age and gender matched healthy children,and collected their venous blood and microbiome samples of nasal and anal swab. Then, CU subjects will be given vitamin D or placebo for 6 months in a randomized, double-blind way. After six months of follow-up, their blood, nasal cavity, and intestinal bacterial samples were taken. All microbial analysis, allergen detection, vitamin D concentration, VDR, DBP genotype will be analyzed by the core laboratory and bioinformatics center of CMUH.
The investigators believe this study can answer the cause-effect relationships of microbiota and vitamin D in the development of CU, and design a microbiota-related preventive and treatment strategy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urticaria
Keywords
Vitamin D, human microbiome, vitamin D receptors and vitamin D binding protein
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Treatment group
Arm Type
Experimental
Arm Description
Vitamin D (2000IU/day) for 6 months
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Other
Intervention Name(s)
Vitamin D
Intervention Description
Vitamin D (2000IU/day) for 6 months
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Levels of vitamin D
Description
Vitamin D will be measured in a blood sample by ELISA to determine baseline status.
Time Frame
Month 0
Title
Levels of vitamin D
Description
Vitamin D will be measured in a blood sample to follow the change from baseline in vitamin D level at month 6.
Time Frame
Month 6
Title
Single nucleotide polymorphism of vitamin D receptor and vitamin D binding protein.
Description
Single nucleotide polymorphism (SNP) genotyping will be performed in a blood sample by using TaqMan SNP genotyping assays.
Time Frame
Month 0
Title
Microbiome Microbiome
Description
Nasal and anal swabs will be used to detect respiratory and intestinal microbiome by using 16S rRNA sequencing to determine baseline status.
Time Frame
Month 0
Title
Microbiome Microbiome
Description
Nasal and anal swabs will be used to detect respiratory and intestinal microbiome by using 16S rRNA sequencing,and to follow the change from baseline in microbiome at month 6.
Time Frame
Month 6
Title
Total IgE
Description
Plasma total IgE concentration will be measured by microparticle immunoassay (IMx analyzer, Abbott Laboratories, Abbott Park, IL) and ELISA to determine baseline status.
Time Frame
Month 0
Title
Total IgE
Description
Plasma total IgE concentration will be measured by microparticle immunoassay (IMx analyzer, Abbott Laboratories, Abbott Park, IL) and ELISA to follow the change from baseline in total IgE at month 6.
Time Frame
Month 6
Title
Allergen-specific IgE
Description
Plasma allergen-specific IgE will be measured by BioIC ®.
Time Frame
Month 0
Secondary Outcome Measure Information:
Title
Quality of Life Assessment
Description
Patients will rate their CU symptoms and the impact of their CU on various aspects of their lives. Each question is scored from 0 (not at all) to 3 (very much). Overall score, on scale of 0 to 57.
Time Frame
Month 0 to Month 6
Title
The Urticaria Activity Score 7 (UAS7)
Description
The Urticaria Activity Score 7 measures number the weekly average of hives and pruritus measured twice a day. It scores from 0 to 42.
Time Frame
Month 0 to Month 6
10. Eligibility
Sex
All
Minimum Age & Unit of Time
0 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Experimental group: patients with chronic spontaneous urticaria under the age of 18 .
Control group: healthy children under the age of 18 (eg, healthy siblings of sick children).
Exclusion Criteria:
Recruit patients who have used antibiotics, systemic steroids, and immunosuppressants in the previous month.
Patients with C1 esterase inhibitor deficiency, lymphocytopenia, thrombocytopenia, severe diseases involving heart, liver, or kidney, metabolic disease, or autoimmune disease.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiu-Yao Wang, MD
Phone
886422052121
Ext
4131
Email
aim.cmuh@gmail.com
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
Jiu-Yao Wang, MD
Phone
886422052121
Ext
4131
Email
aim.cmuh@gmail.com
12. IPD Sharing Statement
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The Association Between Human Microbiome and Vitamin D in Chronic Urticaria
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