Actively Recruiting

Phase Not Applicable
Age: 4Years - 5Years
All Genders
Healthy Volunteers
NCT06685640

Comparison of Clinical Success of Stainless Steel Crowns and Zirconia Crowns in Primary Molars

Led by Aydin Adnan Menderes University · Updated on 2025-12-22

10

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Evaluation and understanding of clinical success, parental satisfaction and effects on periodontal tissues are the main expected benefits of prefabricated zirconia crowns and prefabricated stainless steel crowns. For a long time, stainless steel crowns have been the restorative material of choice for children's primary and permanent posterior teeth. Today, prefabricated zirconia crowns are more popular than other options because they meet aesthetic expectations and have high mechanical strength. The aim of this study is to evaluate and compare the periodontal health, plaque accumulation, opposing tooth wear, parental satisfaction, and clinical performance (color match, retention, marginal integrity, marginal discoloration, anatomic form, secondary caries, surface roughness, surface gloss and postoperative sensitivity) of pediatric prefabricated stainless steel and zirconia crowns applied after pulpotomy to asymptomatic, multifaceted, deep carious primary mandibular second molars.

CONDITIONS

Official Title

Comparison of Clinical Success of Stainless Steel Crowns and Zirconia Crowns in Primary Molars

Who Can Participate

Age: 4Years - 5Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 4 to 5 years
  • Systemically healthy children
  • Positive or extremely positive behavior according to the Frankl behavior scale
  • Asymptomatic primary mandibular second molars with multi-surface deep caries needing pulpotomy
  • No history of spontaneous pain
  • Bleeding at pulpotomy site controllable within 3 to 5 minutes
  • Opposing teeth in occlusal contact
  • No periodontal-related attachment loss
  • No abscesses or fistulas on primary second molars
  • Children who agree verbally and in writing to participate and attend follow-ups
Not Eligible

You will not qualify if you...

  • Having a systemic disease
  • Periapical infection, abscess, or mobility in primary second molars
  • Active periodontal disease
  • Malocclusion or missing opposing tooth
  • Primary second molars with pathological internal or external resorption
  • Physiological root resorption exceeding one-third of the root
  • Children with bruxism or unilateral chewing habits

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

Adnan Menderes University

Aydin, Aydın, Turkey (Türkiye), 09100

Actively Recruiting

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Research Team

K

Kadriye Görkem Ulu Güzel, Doç. Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

2

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