Comparison of pain levels in nasopalatine nerve blocks using two different techniques
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
研究概览
简要总结
Minimizing discomfort during dental anesthetic injection may favor patient compliance with dental treatment. The aim was to compare pain levels between the conventional injection and the Morpheus® device for the nasopalatine nerve block during the puncture, needle introduction, and local anesthetic (LA) deposition. A crossover, double-blind, randomized clinical trial was carried out involving 32 participants. Group I comprised the conventional syringe (control group), while Group II comprised the Morpheus® device (experimental group). The total volume of LA administered was 0.6 mL for both techniques. The study was developed in two sessions, two weeks apart. The pain was assessed using a 100-mm Visual Analog Scale (VAS). The intragroup analyses were performed using the Friedman’s test and Durbin-Conover's post hoc test. The Wilcoxon test was used for intergroup analyses. The significance level was set at p < 0.05. Intragroup analyses showed statistical differences within Group I and II (p < 0.001 and p = 0.003, respectively). All the evaluated moments of both injection techniques differed statistically, except between the needle introduction and LA deposition moments in Group II (p = 0.526). In the intergroup analyses, participants of Group I presented higher pain levels, experiencing the highest pain at the LA deposition moment (median 58; 46 - 62). Pain levels were statistically significant between all the corresponding moments of the groups (p < 0.001). Computerized injection with the Morpheus® can be effectively employed to increase comfort during anesthetic injections and patient compliance with dental treatments
研究设计
- 研究类型
- Intervention
入排标准
- 年龄范围
- 18Y 至 30Y(—)
入选标准
- •Both genders; age between 18 and 30 years; any ethnicity; any marital status; any nationality; any place of birth; with previous experience of local anesthesia without intercurrences; not having undergone infiltrative anesthesia in the region in the two weeks prior to the study; and not having used any medication capable of altering pain perception in the two weeks prior to the study
排除标准
- •Age lower than 18 years or higher than 30 years old; pregnant or lactating women; history of hypersensitivity to the drugs used in the study; alcohol abuse or drug dependence; psychiatric disorders or systemic diseases; being under treatment with CNS-acting drugs; use of drugs capable of altering pain perception in the two weeks preceding the study; and moderate anxiety or higher (over 9), based on Corah's Dental Anxiety Scale
