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Efficacy of Dipotassium Glycyrrhizinate Emollients in the Maintenance Treatment of Adult Atopic Dermatitis

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Xuzhou Medical University

Status

Completed

Conditions

Adult Atopic Dermatitis

Treatments

Drug: White yu green skin lotion

Study type

Interventional

Funder types

Other

Identifiers

NCT06565117
XYFY2022-KL323-02

Details and patient eligibility

About

To investigate whether emollients containing dipotassium glycyrrhizinate have a sustained improvement in the clinical severity of mild to moderate atopic dermatitis in adult.

Full description

Atopic dermatitis (atopic eczema, AD) is a common skin inflammatory disease, dry skin and itchy skin is a significant symptom of most AD, often accompany patients for life, seriously affecting the physical and mental health and work life of patients. The number of AD patients is increasing worldwide, while the prevalence rate in China has increased more significantly in the past 10 years. It is characterized by persistent skin dryness and a reduced function of the skin as a barrier to the external environment. Encourage the free use of moisturizers (emollients) as a baseline treatment for AD and add anti-inflammatory therapy as needed. Currently, topical corticosteroids are still the first-line treatment options. However, studies have confirmed that patients with AD are cautious about the use of topical corticosteroids. Maintaining the humidity of the skin and restoring the barrier function of the skin is the basis of the treatment of atopic dermatitis. And studies have shown that regular use of emollients can improve skin hydration, restore the skin barrier, reduce the frequency of attacks, and reduce the use of topical corticosteroids. In patients with AD, daily use of moisturizing emollients enhances the response to topical corticosteroid therapy, reduce percutaneous water loss (TEWL), restore the skin barrier and promote hydration, and can prevent or reduce AD attacks by improving the associated skin barrier defects, prolonging the time between AD episodes. The purpose of this study is to see whether emollients have sustained improvement on the clinical severity of adult atopic dermatitis in maintenance phase.

Enrollment

120 patients

Sex

All

Ages

17 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meet the Williams diagnostic criteria
  • SCORAD scores < 50 points, classified according to the severity levels of SCORAD scores, where scores of 0-25 are categorized as mild, and scores of 26-50 are categorized as moderate
  • No gender limit, age between 18-65 years old.

Exclusion criteria

  • Acute disease with erosion, exudation, secondary infection
  • There are currently other active inflammatory skin diseases
  • Antihistamine was used within 2 weeks prior to enrollment
  • Patients treated with emollients and receiving topical drugs (such as glucocorticoids and calcineurin inhibitors) within 1 week before enrollment
  • Patients have used phototherapy, systemic corticosteroids, immunosuppressants (such as cyclosporine, azathioprine, or immunoglobulin, etc.) within 4 weeks before enrollment
  • The systematic withdrawal time of biological agents or JAK inhibitor (dupilumab, omalizumab, et al) was less than 12 weeks
  • Malignant tumors, chronic systemic diseases (such as diabetes mellitus, hypothyroidism), or other acute and chronic infections
  • Those known to be allergic to the ingredients of emollient or Hydrocortisone cream
  • Patients who have attended or are attending other clinical investigators within three months
  • Patients judged unsuitable by the investigator to participate in this study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

120 participants in 3 patient groups

A:Emollient for systemic application
Experimental group
Description:
Emollient for systemic application
Treatment:
Drug: White yu green skin lotion
B:Emollient was applied locally
Experimental group
Description:
Apply skin lotion in locally affected skin areas or in areas previously affected by AD
Treatment:
Drug: White yu green skin lotion
C:No moisturizer
No Intervention group
Description:
No moisturize

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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