Actively Recruiting

Phase Not Applicable
Age: 5Years - 7Years
All Genders
NCT07344038

Bioceramic Putty Versus MTA in Pulpotomized Primary Teeth to be Covered With 3D Printed Resin Crowns Versus Stainless Steel Crown

Led by Alexandria University · Updated on 2026-01-15

60

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

children aged 5 to 7 years with deep carious second primary molars that require vital pulp therapy will be treated using either MTA or bioceramic putty, then will be fully covered using either stainless steel crowns or 3D printed resin crowns.

CONDITIONS

Official Title

Bioceramic Putty Versus MTA in Pulpotomized Primary Teeth to be Covered With 3D Printed Resin Crowns Versus Stainless Steel Crown

Who Can Participate

Age: 5Years - 7Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged from 5 to 7 years
  • Medically healthy children (ASA I)
  • Positive or definitely positive behavior (Frankl's rating scale scores III or IV)
  • Parents/legal guardians must provide written informed consent
  • Deep carious second primary molars with vital pulp and signs of reversible pulpitis
  • Teeth requiring full coverage restorations
  • Cooperative children (Frankl 3 or 4 behavior rating scale)
Not Eligible

You will not qualify if you...

  • History of spontaneous pain
  • Tooth mobility
  • Excessive bleeding from radicular stumps after coronal pulp amputation
  • Radiographic evidence of pathological root resorption, inter-radicular bone loss, periapical pathology, or canal calcifications
  • Previous dental treatment of the involved molar
  • Children with special healthcare needs

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Dentistry, Alexandria University, Egypt

Alexandria, Egypt

Actively Recruiting

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Research Team

Y

yousr nader pediatric dentist specialist, doctorate

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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