Skip to content

Comparative Evaluation of Hydrophilic and Hydrophobic Sealants in Partially Erupted First Molars

Evaluation of Hydrophilic and Hydrophobic Sealants' Retention, Caries Prevention, Microleakage, and Fluoride Release in Partially Erupted First Permanent Molars:A Randomized Controlled Clinical Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07052526
Enrollment
150
Registered
2025-07-04
Start date
2025-07-01
Completion date
2027-04-01
Last updated
2025-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries

Keywords

Hydrophilic sealant;, Fluoride, Microleakage, Caries, Retention

Brief summary

This randomized controlled clinical trial aims to evaluate and compare the retention, caries prevention, microleakage, and fluoride release of three types of pit and fissure sealants-hydrophilic, nanofilled hydrophobic, and conventional hydrophobic-applied to partially erupted first permanent molars in children aged 5 to 7 years. The study uses a split-mouth design and includes both clinical and laboratory evaluations over an 18-month period. Outcomes will assess sealant effectiveness with and without the use of a bonding agent.

Detailed description

This is a randomized controlled clinical trial designed to evaluate and compare the effectiveness of three types of pit and fissure sealants-hydrophilic (Embrace WetBond), nanofilled hydrophobic (DENU Seal), and conventional hydrophobic (Helioseal F)-when applied to partially erupted first permanent molars in children aged 5 to 7 years. The study aims to assess the sealants' clinical retention, their ability to prevent dental caries, microleakage, sealant penetration depth, and fluoride release. A total of 150 children will be randomly assigned to three equal groups of 50 participants each. A split-mouth design will be used: in each group, sealants will be applied with and without bonding agents on opposite sides of the upper or lower arch, allowing intra-subject comparisons. Clinical evaluations will be conducted at 3, 6, 12, and 18 months to assess sealant retention and caries incidence using the modified Color, Coverage, Caries (CCC) Sealant Evaluation System. In addition to the clinical phase, a laboratory phase will be conducted using extracted human premolars. This phase will evaluate microleakage and sealant penetration under a stereomicroscope following dye penetration techniques. Fluoride release will be measured at specified time intervals (1, 7, 14, 21, and 28 days) using an ion-selective electrode in artificial saliva conditions maintained at 37°C. The primary outcomes include sealant retention and caries incidence. Secondary outcomes focus on the degree of microleakage, sealant penetration, and fluoride release. The trial will help determine whether moisture-tolerant sealants offer superior clinical and preventive benefits over traditional hydrophobic materials, particularly in situations where ideal isolation is difficult, such as with partially erupted teeth in young children. The study will be conducted at the Pediatric Dentistry Clinic, Faculty of Dentistry, Mansoura University, and is expected to generate evidence that could improve clinical decision-making in preventive pediatric dentistry.

Interventions

OTHERPrevention

Conventional Hydrophobic Sealant (Helioseal F - Control) will be used as a positive control; applied to partially erupted molars with and without bonding in a split-mouth design.

OTHERPrevention of caries

Embrace WetBond sealant will be applied to partially erupted first permanent molars using a split-mouth design with and without bonding agent.

DENU Seal applied using a split-mouth design to evaluate bonding and non-bonding application outcomes from retention and caries prevention

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Intervention model description

A total of 150 children aged 5-7 will be randomly assigned to three equal groups of 50 participants each

Eligibility

Sex/Gender
ALL
Age
5 Years to 7 Years
Healthy volunteers
Yes

Inclusion criteria

\- Inclusion Criteria: * Cooperative children (Frankl Scale 3) * good oral hygiene (OHI-S Index), * 2 partially erupted 1st molars

Exclusion criteria

* Cavitated caries * fluorosis * hypoplasia * restored teeth

Design outcomes

Primary

MeasureTime frameDescription
Retention18 monthsretention is evaluated using CCC Index (Color, Coverage, and Caries) This scale is used to assess sealant retention and caries status during follow-up evaluations. Score Description Retention Caries Status Interpretation 0 Sealant completely retained no caries Full retention Best outcome 1. Partial sealant loss no caries Partial loss Acceptable 2. Sealant completely lost no caries Total loss Less ideal 3. Sealant partially or totally lost caries present Partial or total loss Worst outcome
Caries18 monthsCaries Incidence: 3, 6, 12, 18 months, t each recall (3, 6, 12 months), evaluate each sealed tooth using the CCC score: If the sealant is completely intact and no caries is visible → score = 0 If the sealant is partially gone but no decay → score = 1 If sealant is lost but still no decay → score = 2 If sealant is lost/partial and there is decay → score = 3

Secondary

MeasureTime frameDescription
Microleakage3 monthsMicroleakage Assessment (lab) - dye penetration . Score Description Microleakage Depth Interpretation 0 No dye penetration 0% of fissure depth Best outcome 1. Dye penetrates into enamel only \<50% of enamel Good 2. Dye penetrates to dentino-enamel junction (DEJ) Reaches DEJ, no dentin Borderline 3. Dye penetrates into dentin Past DEJ into dentin Worst outcome Minimum score: 0 = no leakage Maximum score: 3 = extensive leakage Higher score = worse outcome
Fluoride release2monthsFluoride Release - spectrophotometer (1, 7, 14, 21, 28 days) Fluoride Release Scoring System (Modified Scale for Clinical Correlation) Because fluoride release is continuous and measured in ppm or µg/cm²/day, we can categorize release levels into scores for easier interpretation. Score Fluoride Release Level Typical Range Interpretation 0 High, sustained release \>2 ppm after 1 week Best outcome 1. Moderate release 1-2 ppm after 1 week Good 2. Low release 0.5-1 ppm after 1 week Weak effect 3. Negligible release \<0.5 ppm after 1 week Ineffective

Countries

Egypt

Contacts

Primary ContactDr. Heba Mohamed DEGHID, Master
Heba.pl70@gmail.com2001016684174

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026