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Effectiveness of acupuncture at acupoint BL1 (Jingming) in comparison with artificial tears for moderate to severe dry eye disease: a randomized controlled trial.
Zhang, Xue; Zhang, Bo; Peng, Siyang; Zhang, Guoliang; Ma, Jumei; Zhu, Wenzeng.
Afiliación
  • Zhang X; Department of Acupuncture, South Area of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, No. 138 Xingfeng Street, Daxing District, Beijing, 102618, China.
  • Zhang B; Department of Acupuncture, South Area of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, No. 138 Xingfeng Street, Daxing District, Beijing, 102618, China.
  • Peng S; Department of Acupuncture, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
  • Zhang G; Department of Ophthalmology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
  • Ma J; Department of Ophthalmology, South Area of Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 102618, China.
  • Zhu W; Department of Acupuncture, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China. zhuwenzeng530@163.com.
Trials ; 23(1): 605, 2022 Jul 27.
Article en En | MEDLINE | ID: mdl-35897025
BACKGROUND: The global incidence of dry eye disease (DED) is very high. DED seriously affects the quality of life of patients; however, the current curative effect of medicine for moderate to severe DED is poor. This randomized clinical trial was planned to investigate the effect of acupuncture compared with artificial tears (AT) on moderate to severe DED. METHODS: A randomized clinical trial was performed at 2 hospitals in China. 120 DED patients were randomly equally divided into an acupuncture and an artificial tear group. Either acupuncture or artificial tears was performed for an 8-week period, and a 24-week follow-up was performed. The primary outcome measure was the Schirmer-I test (SIT) change from baseline. The secondary outcome measures included the numerical rating scale (NRS) change from baseline for improvement in ocular symptoms, the ocular surface disease index (OSDI), the tear-film break-up time (TBUT), corneal fluorescein staining (CFS), and acupuncture acceptability. Adverse events also were monitored and documented. RESULTS: For the primary outcome, the mean changes from baseline in the SIT values were significantly different between the acupuncture (5.75 [2.53-9.75]) and AT (0.52 [- 1.18-2.46]) groups at week 8 with a between difference of 5.23 (P < 0.05). Between-group differences of 8.49 in OSDI score change from baseline differed significantly at week 8 (P < 0.05). However, between-group differences of the changes in the average symptom NRS score, TBUT, and CFS did not differ significantly at week 8. Five cases experienced acupuncture-related adverse events. CONCLUSIONS: This randomized clinical trial found that acupuncture at BL1 significantly promoted tear secretion. Acupuncture showed greater benefits than AT for moderate to severe DED. However, the study findings warrant verification. TRIAL REGISTRATION: Registration number: ChiCTR1800015831. Name of trial registry: Efficacy and safety of acupuncture in the treatment of moderate to severe dry eye disease: a randomized controlled trial. Registered on 23 April 2018 ( https://clinicaltrials.gov/ ).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Ojo Seco / Terapia por Acupuntura Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Ojo Seco / Terapia por Acupuntura Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: China