Evaluation of discolouration of anticariogenic material applied in two intervals comparison study.
- Conditions
- Health Condition 1: K029- Dental caries, unspecifiedHealth Condition 2: Z001- Encounter for newborn, infant andchild health examinations
- Registration Number
- CTRI/2024/04/066113
- Lead Sponsor
- Dr Keyuri Patil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Children between the age of 6 to 12 years.
2. Patients with presence of at least one carious lesion in any of
permanent molars extending up to dentin without involving the
pulp will be selected (According to The International Caries
Detection and Assessment System II codes and criteria, code 5
and 6 will be included).
3. Patients with the absence of periodontal disease.
4. Only those children whose parents will give sign on informed
consent for participation in the study.
5. Patients willing to attend the follow-up visits as required for the
trial.
1. Teeth with history of spontaneous pain.
2. Teeth that show signs of arrested carious lesion.
3. Cavitated teeth with pain on percussion, history of swelling, or
sinus tract.
4. Developmental abnormalities of enamel and dentin.
5. Known silver allergy.
6. Medically compromised patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To determine whether immediate or delayed restoration causes <br/ ><br>less discoloration after SDF Application. <br/ ><br>2. To determine whether Composite or Glass Ionomer Cement <br/ ><br>restoration causes less discoloration after SDF applicationTimepoint: 4 weeks, 12 weeks, 24 weeks
- Secondary Outcome Measures
Name Time Method To evaluate longevity of restorations after SDF Application, <br/ ><br>clinically & radiographically.Timepoint: 4 weeks, 12 weeks, 24 weeks