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OpenTrials
Completed

NCT Number: NCT01655342

Assessment of the Effectiveness of Biodentine® in Pulpotomies Primary Teeth

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

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Key information

Conditions

Effectiveness of Biodentine® in Pulpotomies Primary Teeth

Age range

3 year–12 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hadassah Medical Organization

Jerusalem, Israel

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • one or more primary teeth which requires pulpotomy.

Exclusion criteria

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

Treatment and study plan

Primary outcomes

  1. Success of the primary molar pulpotomy

    Time frame: One year

Sponsors and collaborators

Lead sponsor

Hadassah Medical Organization

Other

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2018
Study completion
2018
First posted
Aug 1, 2012
Registry last updated
Mar 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.