Deep Caries, Pulpotomy
Conditions
Keywords
Immature permanent molars,, young permenent molars, pulpotomy, vital pulp therapy, deep caries, Putty MTA, bioceramic MTA
Brief summary
The present study aims to evaluate the clinical and radiographic success of bioceramics putty MTA versus MTA in the pulpotomy of immature permanent molars The main question it aims to answer is: Will the biocermaics putty MTA have higher clinical and radiographic success rates than MTA in pulpotomy of immature permanent molars?
Detailed description
limited clinical trials have reported the clinical and radiographic outcomes after pulpotomy with premixed putty bioceramic MTA and conventional MTA in young permanent molars. MTA has various drawbacks, such as difficulty in handling, long setting time, discoloration of the tooth, and its form as a powder/liquid which raise the responsibility for major material waste. To conquer these issues, bioceramic materials have been developed premixed putty bioceramic MTA is a ready-to-use material for immediate placement with zero waste, saving cost and chair time. Thus, the present study aims to evaluate bioceramic putty MTA's clinical and radiographic success versus MTA in pulpotomy of immature permanent molars.
Interventions
pulpotomy treatment will be done and the premixed bioceramic MTA will be applied in the pulp chamber
DRUGConventional MTA
pulpotomy treatment will be done and powder and liquid MTA will be mixed and applied in the pulp chamber
Sponsors
Cairo University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
6 Years to 8 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients aged from 6-8 years of both sexes have immature permanent molars * with deep carious lesions indicated for pulpotomy. * Restorable young permanent molars with no clinical symptoms of irreversible pulpitis. * Permanent molars without any clinical sign of pulp necrosis including swelling, fistula, pain on percussion, and pathologic tooth mobility. * Permanent molars without any adverse radiographic findings including thickening of the periodontal ligament space, radiolucency at the interradicular or periapical regions * permanent molars without internal and external root resorption, or calcification in pulp tissue.
Exclusion criteria
* Medically compromised patients who have systemic disease. * Uncooperative patients who refuse treatment. * Permanent molars that were previously restored.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Primary Outcome | 24hrs, 1 week | Immediate Postoperative pain \[ Time Frame: one week) post operative pain by Verbal analogue scale.It is a 10 cm long horizontal line with points labeled from 0 to 10 where (0) indicates no pain, (1-3) mild pain, (4-6) moderate pain, and (7-10) severe pain. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Secondary outcome | 6,12 month | The increase in root length, The root lengthening will be assessed in Mm through Digora software |
Countries
Egypt
Contacts
Primary ContactMarwa Ad Hussien, MSD
Outcome results
None listed