The clinical trial aims to compare children's oral health-related quality of life (OHrQL) following caries arrest technique using SDF versus conventional drill and fill in the children with ECC
Early childhood caries (ECC) has been an increasing issue in many countries and has become a significant health problem, especially in socially disadvantaged populations. ECC is a specific form of caries that occurs in children with primary teeth. ECC is characterized as "the early onset of caries in young children with often fast progression which can finally result in complete destruction of the primary dentition". Management of cavitated carious lesions in primary teeth in very young children is time-consuming due to their lack of cooperation, so one of the alternative procedures could be performed with silver diamine fluoride (SDF), to its effectiveness in arresting the activity of carious lesions (cavitated and non-cavitated). It is easy to apply even outside dental offices, and relatively inexpensive solutions can be used particularly when compared to restorative intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
silver diamine fluoride is a colorless with high PH topical fluoride solution of 38% weight/volume use for arresting early childhood caries
Dental composite resins are dental cement made of synthetic resins which were insoluble, of good tooth-like appearance, insensitive to dehydration, and easy to manipulate.
Oral Health to Quality of Life
will be evaluated by a questioner answered by the parents
Time frame: 6 month intervene
The cost effectiveness
will be measured using ICER (incremental cost-effectiveness ratio)
Time frame: 6 month intervene
Parental satisfaction
will be measured by Direct questioning to the parents.
Time frame: 6 month intervene
Side effects
will be measured by Direct questioning to the parents.
Time frame: 6 month intervene
Time of the procedure
will be measured by stopwatch
Time frame: 6 month intervene
Postoperative pain and sensitivity
will be measured by Visual analogue scale
Time frame: 6 month intervene
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.