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Clinical study of acupuncture combined with dupriuzumab in the treatment of moderate and severe AD

Clinical study of acupuncture combined with dupriuzumab in the treatment of moderate and severe AD

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080533
Enrollment
Unknown
Registered
2024-01-31
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

moderate to severe atopic dermatitis

Interventions

control group:Dopliuzumab injection (Manufacturer: Sanofi-aventis groupe, approval number: Import Drug Registration number S20200017, specification: 300mg: 2ml/ branch), subcutaneous injection, the fi
treatment group:On the basis of the control group, TCM acupuncture treatment (including acupuncture and fine medicine moxibustion burning moxibustion) was added.

Sponsors

Chongqing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for AD. 2. SCORAD score was used to evaluate the severity of the disease, moderate AD was defined as 25 ~ 50 points, severe AD was defined as > 50 points. 3. Voluntarily participate in the study and sign the informed consent. 4. The age range is 18 to 75 years old.

Exclusion criteria

Exclusion criteria: 1. There is obvious rupture, erosion, exudation and infection in local skin lesions. 2. Patients with other pruritus diseases. 3. Systemic use of glucocorticoids, immunosuppressants, and JKA inhibitors within the past 2 weeks. 4. Pregnant or lactating women. 5. there are moxibustion and acupuncture treatment contraindications. 6. accompanied by serious cardiovascular and cerebrovascular, liver, kidney, hematopoietic system and other primary diseases, as well as bleeding tendencies.

Design outcomes

Primary

MeasureTime frame
NRS score;

Secondary

MeasureTime frame
EASI score ;DLQI score ;SCORAD score ;eosinophil count;Serum total IgE level;Th1/Th2/Th17/Th22;clinical efficacy;

Countries

China

Contacts

Public ContactQi Song

Chongqing Traditional Chinese Medicine Hospital

406987210@qq.com+86 152 1333 9872

Outcome results

None listed

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