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Clinical efficacy observation of Piyanling liniment in the treatment on neurodermatitis and chronic eczema

Clinical efficacy observation of Piyanling liniment in the treatment on neurodermatitis and chronic eczema

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078027
Enrollment
Unknown
Registered
2023-11-27
Start date
2021-03-25
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Neurodermatitis and chronic eczema

Interventions

Piyanling liniment Group:Spraying Piyanling liniment on the affected skin twice a day, with a dosage of 0.5 ml/cm2 each time
Halcinonide solution Group:Applying Halcinonide solution on the affected skin twice a day, with a dosage of 0.5 ml/cm2 each time

Sponsors

the 71st Group Army Hospital of CPLA Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Neurodermatitis: The inclusion criteria for this study were as follows: patients who met the diagnostic criteria of Chinese Clinical Dermatology, presenting with skin lesions on the head, neck, upper limbs, elbows, palms, dorsal side of the hand, waist, back, lower legs, sacrococcygeal region, etc.; patients exhibiting the main clinical manifestation of itching, along with dense and patchy flat papules or papules that were fused and enlarged, resulting in lichenoid changes; patients aged between 18 and 70 years; patients with a disease duration of more than 1 month, limited range of skin lesions, and the total area of skin lesions not exceeding 10% of the body surface; patients who had not received any oral or topical medications, or other therapies prior to the visit; patients without any history of cardiovascular diseases, nervous system injuries, diabetes, tumors, tuberculosis, or other chronic diseases or mental illnesses. Chronic eczema: The patients met the diagnostic criteria for chronic eczema outlined in "Chinese Clinical Dermatology". The affected areas included the hands, feet, lower legs, elbows, and knees. The main clinical manifestations included thickening and infiltration of the skin, which presented with a brownish-red or grayish color, pigmentation, rough surface, and the presence of a few flaky scales resembling bran. Localized lichenification with clear borders was observed in varying degrees. Papules and vesicles were scattered around the periphery. The patients experienced significant paroxysmal itching, and the disease course exhibited a recurrent pattern. The age range of the patients was between 17 and 71 years. The total area of skin lesions occupied 10% or less of the total body surface area. There were no significant comorbid chronic diseases or mental illnesses observed.

Exclusion criteria

Exclusion criteria: Neurodermatitis: Pregnant or lactating women; skin lesions occurring on the face or external genitalia; skin lesions complicated by bacterial, viral, or fungal infections, or showing signs of systemic infection; occurrence of severe adverse events during treatment, non-compliance with medication instructions, or those deemed unsuitable to continue treatment, making it difficult to assess efficacy or safety due to incomplete data or other factors; patients who did not complete treatment according to the treatment plan; patients who voluntarily request to withdraw from the study. Chronic eczema: Skin lesions occurring in difficult-to-observe areas; patients with concurrent diseases where the skin lesions are not solely caused by chronic eczema; patients with major diseases of the heart, liver, spleen, lungs, kidneys, etc. in the past; pregnant women and breastfeeding women; patients with severe mental disorders who cannot communicate; patients who have recently used topical corticosteroids or other similar drugs; patients who did not comply with medication instructions during treatment, resulting in incomplete data or inability to determine efficacy; patients who self-administered other drugs without permission; patients who subjectively wish to withdraw from the experiment.

Design outcomes

Primary

MeasureTime frame
Skin lesion area;Skin lesion degree;Pruritus degree;Pigmentation degree;Clinical efficacy;

Countries

China

Contacts

Public ContactYang Yang

the 71st Group Army Hospital of CPLA Army

newyyang@163.com+86 187 9542 5217

Outcome results

None listed

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