A clinical trial to study and compare the effects of three different pulpotomy agents ,Platelet rich fibrin, Propolis and Mineral trioxide aggregate in deciduous teeth
Phase 3
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2024/03/064694
- Lead Sponsor
- mesh Kendre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Healthy patient between the age of 4-9 years of age
2.Exposure of vital pulp due to dental caries, approximating to the
pulp radiographically.
3.Teeth should be restorable after completion of the procedure.
4.At least two-third of remaining root length.
Exclusion Criteria
1.Patient with draining sinus.
2.Pathological mobility.
3.History of unprovoked tooth ache or persistent tooth ache.
4.Highly viscous, sluggish, absent haemorrhage observed at radicular.
5.Periapical radiolucency.
6.Dystrophic calcification.
7.Interradicular bone loss.
8.Exfoliating tooth.
9.Presence of symptoms indicative of advanced pulpal inflammation, such as spontaneous pain or history of nocturnal pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Platelet Rich Fibrin and Propolis are better pulpotomy agents in <br/ ><br>primary molar as compared to Mineral Trioxide AggregateTimepoint: 9 months
- Secondary Outcome Measures
Name Time Method clinical and radiographic findings of primary molar <br/ ><br>teeth treated with Platelet Rich Fibrin, propolis, MTATimepoint: 9 months