Comparative Evaluation of SMART Hall Technique Vs. Conventional SS Crown in Primary Molars: a Randomized Clinical Trial

Launched by C K S TEJA INSTITUTE OF DENTAL SCIENCES & RESEARCH · Jun 6, 2024

Keywords

ClinConnect Summary

This clinical trial is studying two different methods for treating cavities in children's back teeth (primary molars). One method is the traditional stainless steel crown (SSC), which involves more drilling and can be uncomfortable. The other is a newer approach called the SMART Hall technique, which is less invasive and aims to preserve more of the child's natural tooth. This trial will compare how well these two techniques work in treating cavities, how much time each treatment takes, and how children feel during and after the procedures.

To participate, children aged 3 to 9 years old with specific types of cavities in their primary molars may be eligible. Parents or guardians need to give their consent and ensure their child can attend follow-up appointments. Throughout the study, children will receive either the SMART Hall technique or the SSC, and their progress will be monitored over three and six months. The goal is to find out which method is better for keeping children's teeth healthy while making the treatment as comfortable as possible.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Children aged 3 to 9 years old.
• • 2. Presence of occluso-proximal carious lesions (ICDAS CODE 3/4/5) in one or more primary molars, confirmed through clinical examination and radiographic assessment.
• • 3. Requirement for restorative treatment in the form of either the SMART Hall technique or standard stainless steel crown (SSC) restoration, as determined by clinical assessment.
• • 4. Willingness and ability of the parent/guardian to provide informed consent and ensure the child's attendance at follow-up appointments.
• • 5. Adequate cooperation of the child during dental treatment and evaluation procedures, as determined by the clinician.
• Exclusion Criteria:
• • 1. Presence of severe systemic medical conditions (e.g., uncontrolled diabetes, immunodeficiency disorders) that may compromise treatment outcomes or pose risks during dental procedures.
• • 2. Use of medications known to interfere with dental treatment or healing, such as anticoagulants or immunosuppressants, unless medically managed and deemed safe by the treating healthcare provider.
• • 3. History of adverse reactions to dental materials or procedures that may contraindicate participation in the study.
• • 4. Inability of the child to tolerate local anesthesia or undergo dental treatment due to psychological, behavioral, or developmental factors.
• • 5. Presence of extensive dental caries or additional oral pathologies requiring urgent or specialized dental care beyond the scope of the study.