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The clinical comparison of two methods for pereventive resin restoration of young permanent teeth

Not Applicable
Conditions
dental caries.
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Registration Number
IRCT20100125003168N4
Lead Sponsor
Reasearch Vice-Chancellor- Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
42
Inclusion Criteria

group of 6-12 years of age
presence of permanent teeth of the first molar in the lower jaw on both sides with minor decay at the occlusal level
evidence of oral hygiene at home
patient collaboration and acceptance of treatment
no therapeutic treatment has been performed on the teeth previously
possibility of isolation by cotton roll and suction

Exclusion Criteria

history of medical illness that may interfere with treatment
drug affecting the saliva and its quality
history of allergy to any of the restorative materials
uncooperation patient

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The retention of restoration. Timepoint: 3 and 6 months. Method of measurement: exploration and observation.
Secondary Outcome Measures
NameTimeMethod
The working time. Timepoint: 3 and 6 months. Method of measurement: exploration and observation.
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