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2毫克/毫升的迪卡皮诺漱口水预防牙龈炎的疗效。

The efficacy of Decapinol mouthwash 2 mg/mL in preventing gingivitis.

作者信息

Yeung S, Groenlund C, Chapple C, Kemm A, Spencer R, Grossberg D, Newell P, Fitzpatrick J, Kelty E, Movert R

机构信息

Department of Preventive Dentistry, University of Sydney, NSW, Australia.

出版信息

Aust Dent J. 1995 Aug;40(4):220-5. doi: 10.1111/j.1834-7819.1995.tb04798.x.

Abstract

In vitro studies and early clinical trials have shown promising results for Delmopinol HCl solution as an effective mouth rinse for reducing experimentally induced gingivitis in the absence of mechanical plaque control. The efficacy of Decapinol mouthwash 2 mg/mL (Delmopinol HCl) in preventing gingivitis in a double-blind, randomized clinical study with parallel group design was studied. Forty-seven healthy young adults were randomly assigned to the Delmopinol or placebo groups. After an initial period of four weeks of intensive oral hygiene including bi-weekly professional cleaning of the teeth and oral hygiene instruction, all subjects achieved a low degree of gingivitis or a plaque score close to zero. At baseline, Bleeding on Probing, Modified Gingival Index and Plaque Index were recorded and the teeth were professionally cleaned. All forms of plaque control were then suspended and subjects were supervised in a one-minute rinsing of Decapinol mouthwash 2 mg/mL or placebo twice daily. Measurements of efficacy variables were then repeated after two and three weeks treatment and adverse events were recorded. After the study period of three weeks all previous plaque control measures were resumed. At week four, all subjects were reassessed for the resolution of gingival inflammation and where residual gingival inflammation persisted, appropriate treatment was given. Only mild and short-lasting adverse events were noted for the use of Delmopinol in the study period. However, for all teeth sites measured, significant differences between Delmopinol and placebo groups were found in Bleeding on Probing (p < 0.05) and Plaque Index (p < 0.0005).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

体外研究和早期临床试验表明,在没有机械性菌斑控制的情况下,盐酸地莫匹醇溶液作为一种有效的漱口水用于减轻实验性诱发的牙龈炎,已显示出有前景的结果。在一项采用平行组设计的双盲、随机临床研究中,对浓度为2 mg/mL的Decapinol漱口水(盐酸地莫匹醇)预防牙龈炎的疗效进行了研究。47名健康的年轻成年人被随机分配到地莫匹醇组或安慰剂组。在最初为期四周的强化口腔卫生期,包括每两周进行一次专业牙齿清洁和口腔卫生指导后,所有受试者的牙龈炎程度都较低或菌斑评分接近零。在基线时,记录探诊出血、改良牙龈指数和菌斑指数,并对牙齿进行专业清洁。然后暂停所有形式的菌斑控制,监督受试者每天两次用2 mg/mL的Decapinol漱口水或安慰剂进行一分钟的漱口。在治疗两周和三周后重复测量疗效变量,并记录不良事件。在为期三周的研究期结束后,恢复之前所有的菌斑控制措施。在第四周,对所有受试者重新评估牙龈炎症的消退情况,对于仍存在残留牙龈炎症的情况,给予适当治疗。在研究期间,使用地莫匹醇仅出现了轻微且持续时间短的不良事件。然而,对于所有测量的牙齿部位,地莫匹醇组和安慰剂组在探诊出血(p < 0.05)和菌斑指数(p < 0.0005)方面存在显著差异。(摘要截断于250字)

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