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Efficacy and safety of Compound Glycyrrhizin Capsules in patients with localized chronic eczema: a multi-center, randomized, double blind, placebo controlled clinical trial

Efficacy and safety of Compound Glycyrrhizin Capsules in patients with localized chronic eczema

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011511
Enrollment
Unknown
Registered
2017-05-27
Start date
2015-07-01
Completion date
Unknown
Last updated
2017-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

localized chronic eczema

Interventions

Compound Glycyrrhizin Capsules:take Compound Glycyrrhizin Capsules 75mg, 3 times a day
apply Mometasone Furoate onitment once a day
placebo capsule group:take placebo Capsules 75mg, 3 times a day

Sponsors

Department of Dermatology, Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. aged from 18-80 years male and female; 2. Clinically Diagnosed localized chronic eczema, Skin involvement for 5% to 15% of body surface areapatients; 3. The disease has no obvious cause; 4. Participant fully understands the content of the clinical trial, is willing to attend the research voluntary andsign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. eczema infected with the bacteria, viruses, or fungi; 2. during gestational and lactation period; 3. patients who are allergic to any ingredient of the drug to be studied; 4. Have severe hepatic disease, kidney disease, hematological system diseases, autoimmune disease,chronic severe infectious disease,diabetes, mental illness, drug addiction, alcoholism; 5. have a history of malignancy or any severe or uncontrolled systemic disease; 6. apply corticosteroids cream within 2 weeks;have taken systemic corticosteroids or other systemic immune inhibitors (e.g. Tripterygium wilfordii et al.) within 4 weeks; 7. rash on face, skin folds such as anus, vulva; 8. Skin lesions with a total area of more than 15% of the body surface area or less than 25 cm2; 9. other reasons that researchers think that should not be selected.

Design outcomes

Primary

MeasureTime frame
EASI;

Secondary

MeasureTime frame
Pruritus;adverse event;Symptom score changing;

Countries

China

Contacts

Public ContactLinfeng Li

Department of Dermatology, Beijing Friendship Hospital, Capital Medical University

zoonli@sina.com+86 13693620186

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026