Health Condition 1: K029- Dental caries, unspecified
Conditions
Interventions
Intervention1: Bioceramic Putty (cerafill Putty): It is pre-mixed, ready-to-use bioceramic material composed of tricalcium silicate, calcium aluminate, calcium oxide, zirconium oxide, iron oxide, sili
Sponsors
Dr Ayushi Chrungu
Eligibility
Inclusion criteria
Inclusion criteria: 1.Systemically healthy patients (Category American Society of Anesthesiologists class 1) (ASA House of Delegates 2014) between age group of 18-40 years with maxillary or mandibular mature permanent carious teeth with radiographic and clinical evidence of symptomatic irreversible pulpitis will be included in the study. 2.Healthy gingiva with no swelling or sinus tract. 3.Active bleeding pulp tissue observed upon access opening and in all canals after full pulpotomy and hemostasis achieved within 5 min following full pulpotomy. 4.Radiographic evaluation showing a normal periapical index (PAI-1)24 5.A written informed consent will be taken from all the patients and only those patients ready to sign the consent form, willing to participate and come for multiple visits for follow up will be included in the study.
Exclusion criteria
Exclusion criteria: 1. Teeth which are non-restorable, necrosed, badly broken or with developmental anomalies, heavy occlusal load, cracks or vertical root fractures will be excluded. 2. Teeth which are periodontally compromised, present with localized gum swelling or showing evidence of sinus tracts, pus discharge and weeping canals will be excluded. 3. Radiographic evidence of inter radicular lesions, internal external root resorption, open apex or pulp stone in pulp chamber will be excluded from the study. 4. Pregnant and lactating women will be excluded. 5. Intraoperative Evaluation If the remaining pulpal tissue displayed a pale yellow, dark brown coloration, it will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To evaluate the treatment outcome of Bioceramic Putty clinically and radiographically as a pulpotomy agent in mature permanent molars with symptomatic irreversible pulpitis at base-line 24hours,2weeks ,6months and 1 year period 2.To evaluate the treatment outcome of Injectable Bioceramic clinically and radiographically as a pulpotomy agent in mature permanent molars with symptomatic irreversible pulpitis at base-line 24hours,2weeks ,6months and 1 year period. 3.To compare the treatment outcome of Bioceramic Putty with Injectable Bioceramic clinically and radiographically as pulpotomy agent in mature permanent molars with symptomatic irre-versible pulpitis at baseline 24hours,2weeks ,6months and 1 year period Timepoint: Baseline 24hours,2weeks ,6months and 1 year period | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactDr Ajay Singh Rao
KM Shah Dental College And Hospital
Outcome results
None listed