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Theracal Pulpotomy in Primary Molars

A

Ain Shams University

Status and phase

Completed
Phase 4

Conditions

Deep Caries

Treatments

Drug: Formocresol
Drug: Theracal LC

Study type

Interventional

Funder types

Other

Identifiers

NCT04397094
FDASU-Rec ID 101612

Details and patient eligibility

About

Light cured silicate based cement (theracal LC) pulpotomy was compared to formocresol pulpotomy in primary molars.

Full description

sixty primary molars were either treated with Theracal LC or formocresol pulpotomy. Teeth were followed up clinicaly and radiographically for 12 months.

Enrollment

60 patients

Sex

All

Ages

4 to 7 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy, cooperative children
  • mandibular primary molars with vital pulp exposures

Exclusion criteria

  • clinical or radiographic evidence of irreversible pulpitis
  • physiological root resorption

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Theracal LC
Experimental group
Description:
Theracal LC was used as a medicament to cover root stumps of asymptomatic thirty primary molars with vital pulp exposures. Teeth were followed up clinically and radiographically for 12 months.
Treatment:
Drug: Theracal LC
Formocresol
Active Comparator group
Description:
Formocresol was used as a medicament to cover root stumps of asymptomatic thirty primary molars with vital pulp exposures. Teeth were followed up clinically and radiographically for 12 months.
Treatment:
Drug: Formocresol

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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