Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth

NCT01655342 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 58

Last updated 2020-03-04

No results posted yet for this study

Summary

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

Conditions

  • Effectiveness of Biodentine® in Pulpotomies Primary Teeth

Sponsors & Collaborators

  • Hadassah Medical Organization

    lead OTHER

Eligibility

Min Age
3 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2018-12-01
Completion
2018-12-01

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01655342 on ClinicalTrials.gov