Skip to content

Clinical Observation of Nerve Block Therapy in the Treatment of Refractory Neurodermatitis: A Single-Center Randomized Controlled Trial

Clinical Observation of Nerve Block Therapy in the Treatment of Refractory Neurodermatitis: A Single-Center Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112728
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-11-21
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Neurodermatitis

Interventions

Group B:Group B: Conventional treatment plus liposomal bupivacaine nerve block: Oral ebastine tablets, 10 mg QD (once daily) + topical halometasone cream (as needed) + single-dose liposomal bupivacain
Group C:Group C: Liposomal bupivacaine nerve block alone: Enrolled patients receive a single-dose liposomal bupivacaine (133 mg) ultrasound-guided nerve block at the Anesthesia and Surgery Center, adm
Group A:Group A: Conventional treatment group (oral antihistamine + topical corticosteroid): Oral ebastine tablets, 10 mg QD (once daily) + topical halometasone cream (as needed).

Sponsors

The Seventh Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients meeting the diagnostic criteria for neurodermatitis, with clearly defined lesion locations, and exclusion of other concurrent dermatological conditions; 2.Patients who have failed or relapsed after treatment with potent topical corticosteroids, or have relapsed following other guideline-recommended standard therapies; 3.Age 18-65 years; 4.With no significant comorbid systemic diseases, such as respiratory, circulatory, or immune system disorders

Exclusion criteria

Exclusion criteria: 1.Allergy to local anesthetics; 2.Concurrent severe dermatological or neurological disorders; 3.Unwillingness to provide informed consent; 4.Pregnancy or lactation; 5.Presence of psychiatric disorders

Design outcomes

Primary

MeasureTime frame
Numerical rating scale,NRS;

Secondary

MeasureTime frame
Interleukin-31;Interleukin-4;Interleukin-13;Standardized Scoring Form;Dermatology Life Quality Index (DLQI);Calcitonin gene related peptide(CGRP);

Countries

China

Contacts

Public ContactChi Xinjin

The Seventh Affiliated Hospital Sun Yat-sen University

chixinjin@yeah.net+86 13903010076

Outcome results

None listed

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