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Clinical Observation of Topical Lidocaine Cream Combined With Moisturizing Cream in the Treatment of Atopic Dermatitis

Clinical Observation of Topical Lidocaine Cream Combined With Moisturizing Cream in the Treatment of Atopic Dermatitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07067541
Enrollment
25
Registered
2025-07-16
Start date
2023-10-01
Completion date
2024-01-31
Last updated
2025-07-16

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

Conditions

Atopic Dermatitis

Brief summary

Twenty-five patients with atopic dermatitis applied lidocaine cream plus a moisturizer to the right limb and lidocaine cream alone to the left limb, twice daily for four weeks.

Interventions

DRUGControl lidocaine cream

lidocaine cream alone

DRUGExperimental lidocaine cream + moisturizer cream

lidocaine cream + moisturizer cream

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Male or female patients aged 18-65 years. 2. Clinical diagnosis of atopic dermatitis according to the 2020 Guidelines for the Diagnosis and Treatment of Atopic Dermatitis in China (symmetrical eczematous lesions for ≥6 months plus personal/family atopy history or elevated IgE/eosinophilia). 3. Voluntarily signed informed consent form.

Exclusion criteria

1. Active heart, liver, kidney, or other serious systemic illness. 2. History of viral or bacterial infection within 1 month prior to enrollment. 3. Immunocompromised patients or those receiving systemic immunosuppressive therapy. 4. Known allergy to lidocaine, moisturizer components, or any study-related topical agents. 5. Pregnant or breastfeeding women. 6. Use of topical corticosteroids or calcineurin inhibitors within 2 weeks prior to enrollment.

Design outcomes

Primary

MeasureTime frameDescription
change in SCORAD (SCORing Atopic Dermatitis) from baseline4 weeksFor each patient, a score will be obtained at baseline, after 4 weeks. The minimum score is 0 (best outcome) and the maximum score is 103 (worst outcome).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026