Clinical Trials Directory

Trials / Completed

CompletedNCT02782390

Efficacy of Hall Technique in Atypical Lesions on Primary Teeth

Efficacy of Hall Technique in Atypical Lesions on Primary Teeth: Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
364 (actual)
Sponsor
Faculty Sao Leopoldo Mandic Campinas · Academic / Other
Sex
All
Age
4 Years – 9 Years
Healthy volunteers
Not accepted

Summary

Atypical carious cavities could be defined as carious lesions in more than 2 surfaces of the same tooth. Dental practitioners have shown difficulties related to material's maintenance in such type of cavities and therefore, several treatment options have been used. However, most of them have shown a great failure percentage. A randomized clinical trial will be developed with the objective of assessing the Hall technique in comparison with the composite resin incremental technique in 364 primary molars' atypical carious lesions of children between 4 and 9 years old. Initially, two previously calibrated examiners will perform caries diagnosis by means of visual assessment and intraoral examination. Selected teeth will be randomly allocated into two groups. Teeth in the first group will be submitted to prefabricated stainless steel crowns treatment (Hall technique); and the other, to composite resin incremental technique, which will be always placed under rubber dam isolation. Lesions' clinical and radiographic follow-up will be conducted after 6 and 12 months. Treatment's efficacy will be assessed by means of four main outcomes: 1. Longevity, marginal adaptation, possible modification in patients' vertical dimension, and caries lesion progression; 2. Patient-focused criteria (satisfaction, discomfort and quality of life impact); 3. cost-efficacy; and 4. Treatment-related parents', children' and operators' perception. Other variables could be further analysed as secondary outcomes, such as techniques performing time among operators, impact of the socio-economic characteristics on restorations' longevity, and restorations' type impact on the antagonist tooth. Comparisons between groups will be addressed using the Kaplan-Meier survival test as well as Long-Rank test. Cox Regression will be used to enable the assessment of other variables' influence in the results. Significance value of 5% will be adopted for all analysis.

Conditions

Interventions

TypeNameDescription
OTHERDental Restoration with Stainless CrownLesions allocated to this group will be treated with stainless dental crowns according to the Hall Technique protocol (Evans \& Innes, 2010).
OTHERDental Restoration with Composite ResinSurfaces allocated to this group will be treated with composite resin (Z250, 3M ESPE, USA) according to the manufacturer's instructions. Initially, local anesthesia and rubber dam adaptation will be performed. Then, 37% phosphoric acid will be applied on the surface for 15 seconds, followed by spray of water/air for at least 15 seconds. Then, the adhesive system (Single Bond, 3M ESPE, USA) will be applied and light cured according to the manufacturer's instructions. Finally, composite resin (Z250, 3M ESPE, USA) will be applied and light cured according to the manufacturer's instructions.

Timeline

Start date
2016-06-01
Primary completion
2016-11-01
Completion
2017-12-01
First posted
2016-05-25
Last updated
2022-06-02

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02782390. Inclusion in this directory is not an endorsement.