Chronic oral candidiasis

Introduction: Oral candidiasis is an infectious disease caused by the growth of Candida colonies and their penetration into oral tissues when physical barriers and host defenses are weakened. It constitutes one of the most common pathologies within the field covered by Dentistry. Candida infections are found in at least 80% of AIDS patients and in a third of HIV infection cases. Systemic diseases such as diabetes and a wide pharmacological arsenal to which the general population is subjected, are other causes of the increase in the prevalence of this disease. In addition, the high prevalence of oral sequelae (hyposialia) in the population over 65 years of age, due to the specific characteristics of this age group, such as multiple pathologies and drug use, explains the presence of this disease in this segment. of the population One of the great difficulties for the study of this disease is the diversity of predisposing factors, which do nothing but throw greater confusion into the results of the different works.
Objective: To evaluate the reduction/suppression of signs and symptoms of oral candidiasis in patients treated with head and neck RT, users of Vacucis or Placebo.
Material and method: Patients will receive information regarding the trial and, if they meet the inclusion criteria and agree to participate in it, they will sign the informed consent. All patients will be informed following the usual care practice of the characteristics of their candidiasis infection as well as the possibilities and alternatives of treatment and their respective efficacy.
A descriptive analysis of the sample in terms of prevalence will be carried out. Categorical variables will be described as frequency and percentage and continuous variables as mean and standard deviation or median and interquartile range depending on their adjustment to normality, which will be calculated with the Kolmogorov-Smirnov test. To study the effect of the vaccine on the evolution of candidiasis, the Chi-square test, Student's t test or the non-parametric Mann-Whitney test will be used. The association of prevalence with CFU in both groups will be analyzed using the ANOVA test. Those values of p < 0.05 will be considered significant.

主要目的：以宜昌东阳光长江药业股份有限公司提供（宜昌东阳光长江药业股份有限公司生产）的氟康唑胶囊（50 mg）为受试制剂，按有关生物等效性试验的规定，与辉瑞制药有限公司（持证商）的氟康唑胶囊（商品名：大扶康®，50 mg，参比制剂）进行生物等效性试验。 次要目的：评价健康男性和女性受试者餐后状态下单次口服氟康唑胶囊受试制剂和参比制剂后的安全性。

主要目的：以宜昌东阳光长江药业股份有限公司提供（宜昌东阳光长江药业股份有限公司生产）的氟康唑胶囊（50 mg）为受试制剂，按有关生物等效性试验的规定，与辉瑞制药有限公司（持证商）的氟康唑胶囊（商品名：大扶康®，50 mg，参比制剂）进行生物等效性试验。 次要目的：评价健康男性和女性受试者空腹状态下单次口服氟康唑胶囊受试制剂和参比制剂后的安全性。