Fissure Sealant

4

Review clinical trials related to Fissure Sealant. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Effect of Different Deproteinizing Agents on the Clinical Success of Fissure Sealants in Primary Teeth

Investigation of the effect of deproteinization agents on the clinical success of non-invasive fissure sealant application, which is a non-invasive method used to prevent caries formation or to stop the progression of initial caries lesions limited to enamel on tooth surfaces thought to be at high risk of caries.

Participants needed: 60
Trial details
Age: 4-6Biological sex: AllType: InterventionalSponsor: Tokat Gaziosmanpasa UniversityUpdated: Jun 4, 2025Locations: 1
Eligibility criteria

Patients between the ages of 4-6 who do not have any systemic problems [+4]

Teeth with fissure sealants [+2]

Status: Recruiting

The Effect of Different Deproteinising Agents on the Clinical Success of Fissure Sealants in Permanent Teeth

Investigation of the effect of deproteinization agents on the clinical success of non-invasive fissure sealant application, which is a non-invasive method used to prevent caries formation or to stop the progression of initial caries lesions limited to enamel on tooth surfaces thought to be at high risk of caries.

Participants needed: 60
Trial details
Age: 6-9Biological sex: AllType: InterventionalSponsor: Tokat Gaziosmanpasa UniversityUpdated: May 23, 2025Locations: 1
Eligibility criteria

Patients between the ages of 6-9 who do not have any systemic problems [+4]

Teeth with fissure sealants [+6]

Status: Not yet recruiting

CARIES ARREST USING SILVER DIAMINE FLUORIDE VERSUS FISSURE SEALANT in OCCLUSAL DENTAL CARIOUS LESIONS: RANDOMIZED CONTROLLED TRIAL

The goal of this randomized clinical trial is to evaluate if Silver Diamine Fluoride (SDF) is a more conservative and effective treatment in preventing the progression of mild occlusal caries compared to fissure sealant in patients aged 20-45 years with incipient molar caries. The main question it aims to answer is: Is SDF more effective in arresting caries progression than fissure sealant? Does SDF prevent the formation of new caries compared to fissure sealant? Researchers will compare SDF treatment to fissure sealant application to see if SDF results in better caries arrest and fewer new carious lesions. Participants will: Be randomly assigned to receive either SDF or fissure sealant. Have follow-up assessments at 1, 3, 6, and 12 months for caries progression, arrest, and new caries formation. Undergo clinical evaluations using visual and tactile examinations to assess caries arrest and progression and using DIAGNOdent laser fluorescence system .

Participants needed: 76
Trial details
Age: 20-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Mar 6, 2025
Eligibility criteria

Patient consulting in the outpatient clinic. [+4]

Tooth mobility. [+7]

Status: Recruiting

The Effect of an Adhesive System on the Retention and Caries Prevention for Fissure Sealants in Permanent Molars

Background: Resin-based fissure sealants (FS) are recommended to prevent pit-and-fissure caries development or prevent the progression of enamel caries lesion to frank cavitation into dentine. There is still limited clinical evidence on the use of adhesive system beneath fissure sealants in permanent molars and its effect on FS retention and caries progression. Aim: The aim of this randomised clinical trial is to evaluate the clinical efficacy of fissure sealants placed with and without prior use of an adhesive system in terms of retention and caries prevention in permanent molars over the period of 2 years. Study design: Children (6-12 years of age) with high caries risk that require sealants in their first permanent molars (ICDAS 0-3) will be selected at the Dublin Dental University Hospital (DDUH). Molars will be stratified according to presence of caries lesions (ICDAS 0 or ICDAS1-3) and randomly allocated according to the study groups (Test group: 17% phosphoric acid + adhesive system + FS; Control group: 17% phosphoric acid + FS). The randomisation unit will be the tooth and more than one tooth can be included per child. All children will be evaluated after 12 and 24 months by calibrated independent examiners. The primary outcome of the present trial is sealant retention over time. Clinical variables such as age, gender, tooth position (upper/lower), caries experience (DMFT/dmft), stage of eruption (erupted/partially erupted) and children's behavior (Frankl scale) will be collected.

Participants needed: 100
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: University of Dublin, Trinity CollegeUpdated: Nov 8, 2024Locations: 1
Eligibility criteria

6 to 12 years of age; [+3]

Presence of any developmental defects [+3]