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Clinical Trials/NCT01655342
NCT01655342
Completed
Not Applicable

Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth.

Hadassah Medical Organization1 site in 1 country58 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Effectiveness of Biodentine® in Pulpotomies Primary Teeth
Sponsor
Hadassah Medical Organization
Enrollment
58
Locations
1
Primary Endpoint
Success of the primary molar pulpotomy
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Clinical and radiographic assessment of Biodentine® as a pulp dressing material for pulpotomy treatment in human primary molars.

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
December 1, 2018
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • one or more primary teeth which requires pulpotomy.

Exclusion Criteria

  • not healthy patients,
  • patients with teeth which requires pulpectomy.

Outcomes

Primary Outcomes

Success of the primary molar pulpotomy

Time Frame: One year

Study Sites (1)

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