Comparing Bond Strength,Microleakage and Clinical Performance of Three Pit and Fissure Sealants
NCT ID: NCT04272866
Last Updated: 2020-02-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
100 participants
INTERVENTIONAL
2019-07-03
2020-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
1. To evaluate and compare the microleakage of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer Fuji Triage sealant) in vitro.
2. To evaluate and compare the bond strength of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer Fuji Triage sealant) in vitro.
3. To clinically evaluate and compare the retention of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer-based Fuji Triage sealant).
4. To clinically evaluate and compare the caries prevention effect of three different fissure sealants(resin-based Clinpro sealant, Moisture tolerant resin-based Embrace WetBond sealant and glass ionomer-based Fuji Triage sealant).
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Clinical Effectiveness of Embrace Wetbond and Clinpro as Pits and Fissure Sealants in Young Permanent Molars
NCT02933463
Investigation of the Incidence of Caries in Pits and Fissures Sealed With Bioactive Sealant Compared to Fluoride Releasing Resin Based Pit and Fissure Sealant
NCT03628729
Comparative Evaluation of Hydrophilic and Hydrophobic Sealants in Partially Erupted First Molars
NCT07052526
Sealing of Initial Occlusal Caries Using Fissure Sealants
NCT05891288
Comparison Between Resin Based and Glass Ionomer Based Hydrophilic Fissure Sealants
NCT05127343
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Informed consent will be signed for each case by the patient's parent or guardian after thorough explanation of the study.
Procedural Steps:
In vivo
1. Teeth will be divided equally into 3 groups randomly according to the type of sealant used.
2. Pit and fissure sealant application will be conducted by a single operator.
3. A thorough oral prophylaxis of both upper and lower arches was done, followed by polishing using a slurry of pumice and rotating brush to ensure removal of debris from fissures.
4. The occlusal surfaces were then thoroughly cleaned with water to remove all traces of pumice. Isolation of permanent first molars will be obtained using cotton rolls and a saliva ejector.
Group 1(Clinpro sealant)Active control
1. The occlusal surface will be dried and etched with 37% phosphoric acid gel for 30 s
2. Thorough rinsing for 30 s using an oil-free air-water syringe.
3. Clinproâ„¢ Sealant then applied with the brush applicator and light cured for 20 s using visible light cure unit.
Group 2(Embrace WetBond sealant)
1. Etching the teeth for 15 seconds with a phosphoric-acid etchant.
2. Then rinse the etchant from the teeth with an air-water spray for 10 seconds,
3. followed by very light drying of the treated surfaces. With Embrace Wet-Bond, the typical dull, frosted appearance of the etched surface is not desired. Rather, the surface should be lightly dried and very slightly moist with a glossy appearance. To accomplish this, a cotton pellet should be used to remove the excess moisture There should be no visible pooling or drops of water on the tooth surfaces.
4. Applying the Embrace WetBond sealant to the occlusal surface using the supplied applicator tip After dispensing, use a brush applicator to place the sealant, covering all pits and fissures and extending onto the cusp ridges. The final sealant thickness upon application should be at least 0.3 mm.
5. After application, light-cure the sealant for 10 seconds, holding the light-curing probe at right angles to the occlusal surface as close as possible using a high-intensity curing light.
Group 3 (Fuji Triage sealant)
1. The occlusal surfaces conditioned with Dentin Conditioner for 20 s and then rinsed for another 20 s, followed by drying by blotting with a cotton pellet and gently blowing with an air syringe. The surfaces appeared moist and not desiccated.
2. Fuji Triage sealant will then applied to the occlusal surface using a plastic-filling instrument and a disposable nylon brush to spread it into the pits and fissures.
3. The material is self-curing, but a light-curing device can be used for 20 to 40 seconds to hasten setting.
4. When the material loses its glossy appearance, one drop of Fuji Coat is dispensed The coating is applied with a brush to the treated surface and adjacent areas, and light curing is applied .
Articulating paper was used to check the occlusion and any premature contacts were adjusted. The patients were instructed not to eat or drink anything for 30 min, and not to bite or chew on hard substances for the rest of the day. The patients were recalled after a time interval of 1 and 6 months to evaluate the retention and development of caries using Modified Simonsen's criteria.
Criteria for evaluation: (Modified simonsen's criteria) Score 0: No loss of sealant and no evidence of caries Score 1: Partial loss of sealant and no evidence of caries Score 2: Partial loss of sealant and evidence of caries. Score 3: Complete loss of sealant and no evidence of caries Score 4: Complete loss of sealant and evidence of caries. On recall at 3 and 6th month interval, the sealants were evaluated by visual and tactile examination with a sharp probe for retention. The teeth were visually inspected for caries. The data obtained were tabulated and subjected to statistical analysis.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
FACTORIAL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group 1
Teeth in this group will be sealed with clinpro sealant
Clinpro sealant
Resin based sealant
Group2
Teeth in this group will be sealed with embrace wetbond sealant
Embrace wetbond sealant
Moisture tolerant hydrophilic resin based sealant
Group3
Teeth in this group will be sealed with triage sealant
Triage sealant
Glass ionomer sealant
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Clinpro sealant
Resin based sealant
Embrace wetbond sealant
Moisture tolerant hydrophilic resin based sealant
Triage sealant
Glass ionomer sealant
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2- Males and Females 3- Age group between 6-9 years 4- Medically free 5- High caries risk children
Exclusion Criteria
2. Uncooperative children.
3. Children with abnormalities in occlusion
4. children with abnormal oral habits
6 Years
9 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sarah Emad Ali El-Din
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sarah Emad Ali El-Din
Instructor at pediatric dentistry department faculty of dentistry ain shams university
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sarah E Alieldin
Role: PRINCIPAL_INVESTIGATOR
Faculty of dentistry ain shams university
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of dentistry ain shams university
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PED 18-9M
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.