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Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth

H

Hadassah Medical Center

Status

Completed

Conditions

Effectiveness of Biodentine® in Pulpotomies Primary Teeth

Study type

Observational

Funder types

Other

Identifiers

NCT01655342
Moran- HMO-CTIL

Details and patient eligibility

About

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

Enrollment

58 patients

Sex

All

Ages

3 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • one or more primary teeth which requires pulpotomy.

Exclusion criteria

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

Trial design

58 participants in 1 patient group

formocresol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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