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Evaluation of Clinical Efficacy of Acupoint Patch Application in the Chronic Persistent Period of Allergic Asthma and Its Impact on Th17/Treg Immune Balance

Evaluation of Clinical Efficacy of Acupoint Patch Application in the Chronic Persistent Period of Allergic Asthma and Its Impact on Th17/Treg Immune Balance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000906
Enrollment
Unknown
Registered
2026-04-09
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Allergic asthma

Interventions

Treatment group:Acupoint application + Budesonide and Formoterol powder inhaler
Control Group:Simulated Patch + Budesonide and Formoterol Powder Inhaler

Sponsors

Shanxi University of Traditional Chinese Medicine Affiliated Acupuncture and Massage Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnosis of mild to moderate chronic persistent allergic asthma; (2) Identified by TCM differential diagnosis as lung and spleen qi deficiency syndrome; (3) Age between 18 and 65 years; (4) No acupoint patch application within the past month; (5) Not participating in other clinical studies; (6) Able to cooperate with all required tests and measurements; (7) Voluntarily participates and signs the informed consent form. Subjects meeting all the above criteria will be included in the study.

Exclusion criteria

Exclusion criteria: (1) Patients in the acute exacerbation phase or clinical control phase of asthma; (2) Pregnant or breastfeeding women; (3) Individuals allergic to Western medicine (e.g., inhaled corticosteroids, etc.); (4) Patients allergic to the patch medication or adjuvants, or with keloid-prone constitution, or with skin trauma, ulcers, or infections at the patch site; (5) Patients with severe organic diseases of the heart, liver, kidneys, or blood system, a tendency to bleed, or other major illnesses; (6) Patients with concurrent infections or other respiratory diseases; (7) Patients with mental illness or cognitive dysfunction who are unable to cooperate with treatment or follow-up; (8) Patients who have participated in other clinical trials within the past 3 months. If any of the above applies, the individual cannot be included in this study.

Design outcomes

Primary

MeasureTime frame
Asthma Control Test (ACT) Questionnaire;

Secondary

MeasureTime frame
TCM Syndrome Score;Adult Asthma Quality of Life Questionnaire Survey (AQLQ) Scoring;Acute exacerbations;Pulmonary function: First-second forced expiratory volume (FEV1), Forced vital capacity (FVC), Peak expiratory flow (PEF);Fractional Exhaled Nitric Oxide (FeNO);

Countries

China

Contacts

Public ContactZhang Tiansheng

Shanxi Province Acupuncture Hospital

Zts910@163.com13466838493

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026