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Primary Teeth Pulp Capping Material

Not Applicable
Conditions
Health Condition 1: K040- Pulpitis
Registration Number
CTRI/2023/09/057966
Lead Sponsor
Dr. Daya Srinivasan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Children aged 4–7 years with previously untreated lower second primary molars in cooperative children with good general health.

2. Children having had deep dentin caries involving occlusal and or occlusoproximal surfaces.

3. Children who were radiographically detected with caries penetration involving approximately 3/4 of the dentin thickness.

4. Children who were considered to have a potential to result in pulp exposure when the entire caries was cleared according to the complete excavation procedure in which the end point of carious tissue removal is the hard dentin.

5. Children whose teeth showed a moderate response to chemical and thermal stimuli.

Exclusion Criteria

1.Teeth showing signs of irreversible pulpitis (such as spontaneous pain, prolonged pain response)

2.Teeth showing pathological mobility,

3.Teeth showing infectious symptoms such as fistula or abscess, and discoloration

4.Presence of radiolucency in the furcation or periapical regions, and internal or external root resorption.

5.Children with systemic problems, congenital abnormalities and special children.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical criteria: Tooth evaluated for presence / absence of pain, swelling, tender on percussion, pathological mobility & gingival sinus tract opening or purulent discharge Radiographic criteria: Evaluated for radiographic radiolucency , furcal involvement, peri apical radiolucency and internal or external resorption. The increase in dentin thickness will be measured using care stream software attached to Radiovisuography keeping cement-enamel junction as a reference .Timepoint: 3, 6,9,12,18, 24 months
Secondary Outcome Measures
NameTimeMethod
Histological criteria:Pulpal inflammation, prescence of tertiary dentin, Odontoblastic integrity will be evaluated. <br/ ><br>Timepoint: After 6 months follow up
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