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Assessment of chemomechanical removal of carious lesions using Papacarie Duo ™: Randomized longitudinal clinical trial.
Article in English | IMSEAR | ID: sea-148737
ABSTRACT

Background:

Chemomechanical removal of carious lesions consists of the dissolution of carious tissue by the application of a natural or synthetic agent, followed by atraumatic mechanical removal.

Aim:

The aim of the present study was to assess the effectiveness of Papacarie Duo® gel in the chemomechanical removal of carious lesions in primary teeth in comparison to the traditional method (low-speed bur). Settings and

Design:

A randomized clinical trial was conducted with 20 children between 5 and 8 years of age. Materials and

Methods:

Two teeth were treated in each child (split-mouth design), with the randomization of two

methods:

Group 1 – chemomechanical caries removal with Papacarie Duo™; and Group 2 – removal of carious dentin tissue using a low-speed bur. Both methods involved restoration with glass ionomer cement and follow up. The following aspects were evaluated time required for the procedure; pain (face evaluation scale); rtention of the restorative material in the cavity; and the presence of secondary caries after 30 days. Statistical Analysis Used Chi-squared test, Student’s t-test, and Wilcoxon test.

Results:

No statistically significant differences between methods were found regarding time required for the procedure (P = 0.13), the occurrence of pain (P = 0.585), or restoration status at the 30-day clinical evaluation (P = 0.713).

Conclusion:

The findings of the present study demonstrate that the two methods achieve similar results. The advantages of minimally invasive treatment, such as chemomechanical caries removal with Papacarie Duo™, are its ease of use, patient comfort, and the fact that it causes less damage to dental tissue.

Full text: Available Index: IMSEAR (South-East Asia) Type of study: Controlled clinical trial Language: English Year: 2013 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Type of study: Controlled clinical trial Language: English Year: 2013 Type: Article