Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01655342

Enrollment

Registered

2012-08-01

Start date

2012-08-31

Completion date

2018-12-01

Last updated

2020-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Effectiveness of Biodentine® in Pulpotomies Primary Teeth

Keywords

pulpotomy, primary teeth, Biodentine®, formocresol

Brief summary

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

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

3 Years to 12 Years

Healthy volunteers

Yes

Inclusion criteria

* one or more primary teeth which requires pulpotomy.

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Success of the primary molar pulpotomy	One year

Countries

Israel

Outcome results