Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth
This trial is active, not recruiting.
|Condition||effectiveness of biodentine® in pulpotomies primary teeth|
|Sponsor||Hadassah Medical Organization|
|Start date||August 2012|
|End date||August 2015|
|Trial size||60 participants|
|Trial identifier||NCT01655342, Moran- HMO-CTIL|
Clinical and radiographic assessment of Biodentine® as a pulp dressing material for pulpotomy treatment in human primary molars.
Success of the primary molar pulpotomy
time frame: One year
Male or female participants from 3 years up to 12 years old.
Inclusion Criteria: - one or more primary teeth which requires pulpotomy. Exclusion Criteria: - not healthy patients, - patients with teeth which requires pulpectomy.
|Official title||Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth.|
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