Abstract | OBJECTIVE: METHODS: This multicenter, randomized, controlled clinical trial on PER will be conducted at three institutions in China. The total study period will be 9 weeks. After a 1-week preparatory screening period, 240 eligible participants with PER will be randomized to receive acupuncture or pharmacotherapy (1:1) for 4 weeks with a 4-week follow-up. The primary outcome will be changes in 7-day average total nasal symptom score. Secondary outcome measures include rhinoconjunctivitis quality of life questionnaire score and total non-nasal symptom score. RESULTS: The presence and seriousness of psychological and emotional impairments should be considered in therapeutic programs for allergic rhinitis. No clinical trial for treating allergic rhinitis via acupuncture regulation of psychological and emotional activities has been reported. CONCLUSION: The findings of the trial will allow us to determine the effects of the mind (Shen)-regulation treatment approach. We will also be able to confirm if the effects of acupuncture are equivalent to those of the conventional drug cetirizine hydrochloride.
|
Authors | Yanping Wang, Sheng Chen, Peng Wang, Cheng Tan, Chang Zhang, Zhihong Shi, Jiping Zhao |
Journal | Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan
(J Tradit Chin Med)
Vol. 34
Issue 3
Pg. 254-60
(Jun 2014)
ISSN: 0255-2922 [Print] China |
PMID | 24992750
(Publication Type: Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Histamine H1 Antagonists, Non-Sedating
- Cetirizine
|
Topics |
- Acupuncture Therapy
- Adult
- Cetirizine
(therapeutic use)
- Female
- Histamine H1 Antagonists, Non-Sedating
(therapeutic use)
- Humans
- Male
- Middle Aged
- Rhinitis, Allergic
- Rhinitis, Allergic, Perennial
(drug therapy, therapy)
- Treatment Outcome
- Young Adult
|