Effects of Fucoidan on the Gut Microbiota in the Patients of Atopic Dermatitis
NCT ID: NCT05437887
Last Updated: 2022-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
40 participants
INTERVENTIONAL
2022-10-04
2024-03-06
Brief Summary
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Detailed Description
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Current treatments for atopic dermatitis include moisturizing agents, antipruritic drugs (such as oral antihistamines), oral and topical steroids, immunomodulators, light therapy, and antibiotic therapy for infections. External use of steroid ointments can easily atrophy the skin and is not recommended for long-term use. Although oral antihistamines can relieve itching, they have the side effect of drowsiness, which can cause an inability to concentrate and trance. In addition, the long-term use of oral steroids has excellent side effects on the endocrine and so on, and it is not suitable for use during infection.
Intestinal bacteria have many effects on the human body, including nutrient absorption, the formation of vitamins and hormones, and the prevention of the formation of pathological colonies. In recent years, the research on the impact of intestinal bacteria on human immune function has become more and more understood. Immunity effects include Segmented filamentous bacteria that promote the differentiation of Th17 and Clostridium spp. that promote the development of regulatory T cells. At the same time, researchers have also found that many diseases, including allergies, asthma, diabetes, obesity, tumors, and neuropathy, may be related to intestinal bacteria. Hothe investigatorsver, whether fucoidan will affect the colony changes in the human gut after taking it has not yet been studied. Our past research discussed that fucoidan could improve atopic dermatitis with immunomodulatory effects, and whether it is related to changes in gut bacteria is unknown.
Purpose:
This study hopes to understand whether improving symptoms in patients with atopic dermatitis by fucoidan is related to intestinal flora change.
Therefore, this prospective trial's results are designed to understand further fucoidan consumption's effect on atopic dermatitis-the effects of gut bacteria in patients.
At the same time, the clinical effect of fucoidan on patients with atopic dermatitis can be tested again.
Specimen collection and testing:
The investigators will get twice stool specimens and blood draw, about 5 c.c. each time, at the beginning and end of the study (at the tthe investigatorslfth the investigatorsek.)
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Fucoidan
All patients are in the experimental group.
Fucoidan
All patients consumed fucoidan.
Interventions
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Fucoidan
All patients consumed fucoidan.
Eligibility Criteria
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Inclusion Criteria
* The age of the patients must be between 6 and 60 years old. Both men and women can participate.
* Symptoms meet the diagnostic criteria of Hanifin and Rajka AD
* The severity of SCORAD (SCORing Atopic Dermatitis) is 25-50 points.
Exclusion Criteria
* Associated with other skin diseases that may cause itching, as determined by a dermatologist.
* Have bacterial infection or are using oral or injectable western medicines such as steroids, antibiotics, leukotriene antagonists and other immunosuppressants; as well as using phototherapy, immunotherapy, hyposensitivity therapy; full month.
* Those who cannot cooperate with taking the medicine on time. Those who are unable to cooperate with filling out the questionnaire, drawing blood, and leaving stool samples.
* Those who have a history of allergy to fucoidan or have had adverse reactions and hyperthyroidism.
* Severe organ dysfunction, such as impaired renal and hepatic function at the time of initial diagnosis (including chronic kidney disease stage III, IV, V and AST, ALT ≥ 3 times the upper limit of normal), cirrhosis or heart failure, by clinician determination.
* Uncontrollable mental problems or other serious systemic diseases.
* Pregnant or breastfeeding women and all women of childbearing age who do not agree to take appropriate contraceptive measures.
6 Years
60 Years
ALL
No
Sponsors
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Chang Gung Memorial Hospital
OTHER
Responsible Party
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YANG SIEN-HUNG
Director of Department of Traditional Chinese Medicine
Principal Investigators
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Sien-hung Yang, Ph.D.
Role: STUDY_DIRECTOR
Chang Gung Memorial Hospital
Locations
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Chang Gung Memorial Hospital
Taoyuan District, , Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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202200413A3
Identifier Type: -
Identifier Source: org_study_id
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