Clinical Trials Logo

Dental Caries in Children clinical trials

View clinical trials related to Dental Caries in Children.

Filter by:

NCT ID: NCT06372561 Recruiting - Clinical trials for Dental Caries in Children

Comparative Evaluation of Melatonin Versus MTA on Vital Pulp Therapy in Young Permanent First Molars: An in Vivo Study

Start date: May 20, 2023
Phase: N/A
Study type: Interventional

The process of dental caries is dynamic and can be either reversible or irreversible depending on the balance between protective and pathologic factors in the oral cavity. Untreated dental caries causes pulpal injury, inflammation, and necrosis. Melatonin plays an essential role in the regulation of bone growth. The actions that melatonin exerts on odontoblasts may be similar to its action on osteoblasts.

NCT ID: NCT06305845 Active, not recruiting - Clinical trials for Dental Caries in Children

Digital Crowns Versus Prefabricated Crowns on Primary Teeth

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

Badly decayed primary molars will be treated by performing the pulp therapy technique indicated, then the patients will be randomized into two groups to receive the restorative intervention. For the intervention group, teeth will be prepared to receive the digital crown after intraoral scanning while for the control group, teeth will be prepared to receive the prefabricated zirconia crowns. Teeth will be followed up clinically for 1 year, at 1, 6 and 12 months.

NCT ID: NCT06290531 Completed - Clinical trials for Dental Caries in Children

Different Methods for Reducing Buccal Infiltration Local Anesthesia Injection Pain

Start date: January 16, 2022
Phase: N/A
Study type: Interventional

Local anesthetic injection is considered one of the most annoying dental procedures. The use of topical anesthesia is considered a routine procedure in the dental clinic especially for children. However, the taste and application procedure of the topical gel may not be pleasant for all children. The introduction of the Buzzy device is considered a distraction measure in the medical field. Alanazi et al., 2019, studied the effect of using the Buzzy device with cold and vibration compared to the conventional infiltration technique using 30-gauge needle. They concluded that the use of the Buzzy device resulted in better patients' acceptance and significantly lower Wong-Baker scores. Ballard et al., 2019, mentioned in their systematic review the efficacy of the Buzzy device for pain management during needle-related procedures, they concluded that the use of the device may be promising. Ghaderi et al., 2013, evaluated the effect of cooling the injection site on pain perception before infiltration of local anesthetics. They found that cooling the injection site before infiltration of local anesthetics in the buccal mucosa for 1 min, reduced pain perceived by pediatric patients.

NCT ID: NCT06286501 Not yet recruiting - Periodontitis Clinical Trials

Targeting of Preventive Treatment for Adolescents at Risk of Oral Diseases

LumoPrevent
Start date: April 18, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to identify adolescent patients that are at risk of developing oral diseases, and to assess if targeted preventive oral treatment with antibacterial dual-light therapy as an adjunctive treatment method can have a positive impact in preventing oral diseases from emerging.

NCT ID: NCT06283108 Recruiting - Clinical trials for Dental Caries in Children

Gurney Journey: Virtual Reality Distraction

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether a software virtual reality (VR) program provided during transportation to anesthesia induction reduces anxiety before the procedure, and compliance in pediatric patients. This study aims to measure the anxiety of patients as they arrive before their procedure, when parting from their parents for transportation to the procedure room, and when anesthesia is provided. Compliance during anesthesia induction will also be monitored. Participants will be randomly placed into to one of two groups. Group 1 will receive standard care from a Certified Child Life Specialist prior to their surgery. Group 2 will receive standard care from a Certified Child Life Specialist and distraction with a novel virtual reality software program.

NCT ID: NCT06280651 Not yet recruiting - Autistic Disorder Clinical Trials

Dietary Impacts on Oral Health in Autistic Children: A Cross-Sectional Analysis

OHIDPAP-CS
Start date: March 25, 2024
Phase:
Study type: Observational

The study aims to explore how dietary habits affect oral health in children with autism. By examining a cross-section of the autistic paediatric population, the research seeks to identify patterns or specific dietary preferences that may contribute to or mitigate oral health issues. This observational study does not intervene in participants' diets but observes existing habits and their oral health outcomes, aiming to provide insights that could guide better dietary recommendations and oral health practices for children with autism.

NCT ID: NCT06280547 Not yet recruiting - Clinical trials for Knowledge, Attitudes, Practice

The Effect of Oral Health Education on Knowledge, Attitude, Practice and Dental Caries Among Egyptian School Children

KAP
Start date: February 29, 2024
Phase:
Study type: Observational [Patient Registry]

Aim of the study Assessing the effect of an oral health education program on knowledge, attitude, practice, and dental caries among a group of school children in a governmental school in Fayoum, Egypt.

NCT ID: NCT06254053 Not yet recruiting - Clinical trials for Dental Caries in Children

Evaluation of Clinical Performance of Zirconomer Restorative

Zirconomer
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

Is zirconomer restorative material more effective than a glass ionomer cement in restoration of primary molars

NCT ID: NCT06187259 Completed - Clinical trials for Dental Caries in Children

Comparative Study Between Smart Bur II and Traditional Carbide Bur in Selective Removal of Caries in Permanent Molars

Start date: April 18, 2019
Phase: N/A
Study type: Interventional

A more biological and conservative technique of caries removal has emerged with minimally invasive restorative dentistry's advent. As a result, Smart Burs II has become a self-limiting, sensitive tool for removing caries. The current study aimed to validate and contrast the polymer burs' efficacy (Smart Burs II) versus conventional burs (Carbide burs) for infected carious dentin's selective removal in permanent first molars. Thirty permanent first molars fulfilling the inclusion criteria were chosen in 8-11 years old children with class I occlusal carious lesions. Group 1 (n=15) and Group 2 (n=15) were randomly assigned to have carious dentin removed utilizing standard carbide bur and a smart Bur II, consecutively. By employing caries detector dye, the effectiveness of caries removal was quantified as 0, 1, 2, 3, 4, or 5. The volume of removed carious tissue was recorded using impression material which was inserted into a calibrated insulin syringe. A statistically significant difference was discovered in the volume of removed carious tissue between both groups, while the efficiency of caries removal using either bur has no significant difference. Smart Bur II was more conservative in the carious dentin's removal than carbide bur. Smart Bur II was as efficient as carbide bur in caries removal.

NCT ID: NCT06174194 Completed - Clinical trials for Dental Caries in Children

Effect of Sugar-Free Chewing Gum Containing Tulsi Extract on Salivary Streptococcus Mutans in a Group of Children

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial was to explore how adding Tulsi extract, a natural plant substance, to chewing gum affects the levels of Streptococcus mutans, type of bacteria that cause dental caries, in the saliva of children aged 4 to 11 years. Participants should not use removable prosthetics or orthodontic appliances and had had not used antibiotics in the 2 weeks preceding sample collection. We want to answer this main question: Can chewing gum with Tulsi extract significantly reduce the number of Streptococcus mutans bacteria in children's saliva? Participants tasks: - Children were asked to chew gum containing Tulsi extract for 5 minutes and then dispose of the gum. - Two salivary samples were collected from each child: one before gum chewing and another 30 minutes after disposing the gum. Researchers compared Streptococcus mutans counts in saliva before and after gum chewing to determine if there is a significant reduction in bacterial colonies.