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A Randomized Controlled Trial on the Preventive Effect of "Inverse Moxibustion" on Seasonal Allergic Rhinitis

A Randomized Controlled Trial on the Preventive Effect of "Inverse Moxibustion" on Seasonal Allergic Rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002624
Enrollment
Unknown
Registered
2025-12-30
Start date
2026-01-05
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Seasonal Allergic Rhinitis

Interventions

Control Group:No Intervention

Sponsors

Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic criteria for moderate-to-severe seasonal allergic rhinitis (SAR); (2) Have a documented SAR history of =2 years, with predictable seasonal onset and currently be in the remission phase; (3) Have a Total Nasal Symptom Score (TNSS) of =4 during the previous year's symptomatic period; (4) Be aged between 18 and 65 years; (5) Voluntarily agree to participate in this clinical study, be able to complete the required scale assessments as instructed, record the use of anti-allergic medications, and provide signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with comorbid upper respiratory diseases such as asthma or bronchitis; (2) Individuals with intolerance to moxa smoke; (3) Those experiencing fainting during moxibustion or strong aversion to moxibustion therapy; (4) Patients with other nasal conditions including chronic rhinitis, sinusitis, nasal polyps, or deviated nasal septum; (5) Individuals with psychiatric disorders, or who are pregnant or lactating; (6) Patients with severe comorbid conditions affecting the cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems; (7) Those currently receiving Western medical treatments, traditional Chinese medicine therapies, or other complementary and alternative therapies for allergic rhinitis; (8) Subjects concurrently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Attack Rate;Total Nasal Symptom Score;

Secondary

MeasureTime frame
Total Non-Nasal Symptom Score;Rhinoconjunctivitis Quality of Life Questionnaire ;Rescue Medication Score ;serum IL-4, IL-5, IL-13 levels; Patient Satisfaction with Preventive Moxibustion;Patient Preference for Preventive Moxibustion;Incidence of Adverse Events;

Countries

China

Contacts

Public ContactDu Shihao

Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences

jimaike@126.com15611676778

Outcome results

None listed

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