Actively Recruiting
SMART With Different Modifications in Asymptomatic Deep Carious Lesions of Primary Molars.
Led by Çanakkale Onsekiz Mart University · Updated on 2025-08-08
150
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aimed to evaluate the clinical success of the 'Silver Modified Atraumatic Restorative Technique '(SMART) with different modifications in asymptomatic deep carious lesions of primary molars.
CONDITIONS
Official Title
SMART With Different Modifications in Asymptomatic Deep Carious Lesions of Primary Molars.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients and parents who agree to participate and sign informed consent
- Children aged between 4 and 9 years
- Healthy children without serious systemic conditions requiring chronic medication use
- Children with at least one untreated asymptomatic cavitated carious lesion in primary molars meeting ICDAS II codes 4, 5, or 6
- No history of spontaneous pain from the affected tooth or teeth
- Patients able to cooperate to complete treatment under clinical conditions
- Teeth must be in a restorable condition
- Primary teeth to be treated should not be expected to naturally fall out within two years
You will not qualify if you...
- Patients and parents who do not agree to participate or sign informed consent
- Known allergy to silver compounds or any dental materials used in the study
- Patients with special healthcare needs or medical conditions
- Primary molars with excessive crown damage that cannot be restored
- Primary molars with bone loss exceeding one-third of the roots
- Primary molars previously treated with root canal or pulpotomy
- Presence of internal or external root resorption in primary teeth to be treated
- Root fracture, ankylosis, or mobility in primary teeth to be treated
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Canakkale Onsekiz Mart University
Çanakkale, Kepez, Turkey (Türkiye), 17100
Actively Recruiting
Research Team
H
HİLAL ÖZTÜRK Research Assistant
CONTACT
B
Burak Çarıkçıoğlu Assoc. Prof.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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