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A clinical trial on acupuncture for hay fever

The efficacy and safety of acupuncture for seasonal allergic rhinitis: a prospective, randomised controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000751279
Acronym
AcupSAR
Enrollment
175
Registered
2009-08-28
Start date
2009-10-12
Completion date
2011-10-20
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Seasonal allergic rhinitis, also known as hay fever, is a common condition with high prevalence in Australia, being most pronounced during spring and early summer when pollen counts are highest. There is no proven cure for hay fever. Many hay fever sufferers seek alternative therapies such as acupuncture. We propose to undertake a rigorous study, using well-established clinical trial methodology, to evaluate the efficacy and safety of acupuncture in the treatment of hay fever.

Interventions

After a two-week run-in period, the subjects will be treated three times per week for four weeks. Four key (common) acupoints and two supplementary acupoints will be used. “Hwato” disposable pre-sterilised needles will be used. The needle will be 0.22 mm in diameter. The length of the needle will depend on the acupoint locations (25 – 50 mm). The duration of each acupuncture session is 25 minutes.

Sponsors

Prof. Charlie Xue
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Age between 18 and 70 inclusive; a history of at least two years of typical symptoms of SAR, or of persistent allergic rhinitis (PAR) with seasonal exacerbation, including watery rhinorrhoea, sneezing, nasal obstruction and nasal and ocular itch. Although it is common for SAR sufferers to be also sensitised to allergens such as house dust mites, seasonal worsening of symptoms markedly increases morbidity and it is considered unlikely that such worsening of symptoms during the period of high grass pollen counts would be due to PAR rather than to SAR. However, a positive skin-prick test to rye grass pollen will be required for all participants.

Exclusion criteria

History of Human immunodeficiency virus(HIV); current pregnancy or breast-feeding; other current active respiratory diseases such as asthma, sinusitis, and rhinitis medicamentosa; pollen desensitization during the last 6 months; nasal polyposis; other structural defects of the upper respiratory tract; hepatitis B or C; and, currently use systemic corticosteroid therapy or anticoagulant medications. Respondents with atopic dermatitis and who are regularly using topical corticosteroids will also be excluded. In addition, subjects who have experienced acupuncture within the last 24 months will be excluded.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026