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A Randomized, Sham-Controlled Trial of Catgut Implantation at Acupoints for the Treatment of Allergic Rhinitis

A Randomized, Sham-Controlled Trial of Catgut Implantation at Acupoints for the Treatment of Allergic Rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002191
Enrollment
Unknown
Registered
2012-05-09
Start date
2012-10-08
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

alleigic rhinitis

Interventions

real catgut implantation at acupoints group:catgut implantation at acupoints
controlled group:sham catgut implantation at acupoints

Sponsors

Teaching Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: According to ARIA (2008 Update), the diagnostic criteria for allergic rhinitis is based upon the coordination between a typical history of allergic symptoms and diagnostic tests. They are: 1. Typical symptoms of allergic rhinitis: rhinorrhoea, sneezing, nasal obstruction and pruritus. Some patients may have ocular symptoms for outdoor allergens. 2. Prick and puncture tests performed by trained health professionals. 3. The blood specific IgE. The time when subjects have above symptoms should last more than one hour on most days. Standardized vaccines (Alutard SQ, ALK- Abelló, Denmark) are used in the test. Oral H1-antihistamines are not permitted before skin test. And skin tests should be read at the peak of their reaction by measuring the wheal and the flare approximately 15 min after the performance of the test.1 Patients who meet the diagnosis of allergic rhinitis will be included in this study. The criteria are: (1) aged between 18-70 years; (2) not be taking part in any other clinical trials; (3) having no previous experience of catgut implantation at acupoints; (4) provide written informed consent.

Exclusion criteria

Exclusion criteria: Patients with any of the following conditions will be excluded: (1) pregnant women or women who are ready to be pregnant in recent half year, women with lactation; (2) patients are receiving immune therapy; (3) patients with other allergic diseases, such as bronchial asthma or allergic purpura; (4) patients with nasal polyposis; (5) heterologous protein allergy; (6) patients with other organic disorders, such as: AIDS, vascular malformation, hypertension, hematologic diseases, diabetes mellitus, malignant tumor, mental disorder; (7) patients with previous experiences of catgut implantation at acupoints; (8) patients who are unwilling to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
Visual analog scale for the measurement of severity;SF-36 questionaire of QOL;serum allergen-specific IgE;nasal inflammatory cells counts(mast cells, eosinophils, basophils);

Secondary

MeasureTime frame
relief medication score;

Countries

China

Contacts

Public ContactZHANG Qin-xiu
zhqinxiu@163.com+86 18980880173

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 24, 2026