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Clinical Retention of Glass Ionomer Sealants Placed With and Without Rubber Dam: a Comparative Analysis

Clinical Retention of Glass Ionomer Sealants Placed With and Without Rubber Dam: a Comparative Analysis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03989687
Enrollment
18
Registered
2019-06-18
Start date
2019-07-01
Completion date
2020-06-30
Last updated
2019-06-18

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

Conditions

Dental Caries in Children

Brief summary

A comparative analysis of glass ionomer sealant placed on permanent molars with and without a rubber dam to assess the retention over a 2 year period.

Detailed description

The purpose of the study is to compare the retention rates of glass ionomer sealants placed on first permanent molars over a period of 2 years. Pediatric patients (under \<10 years of age) will receive a glass ionomer sealant on all four permanent first molars. One side will be randomly selected with rubber dam isolation and the contralateral side will have no rubber dam isolation for the placement of the sealant. Over a 2 year period, every 6 months the sealants will be assessed for retention. The glass ionomer sealant material will be Fuji Triage (GC America). The following dental materials that will be used are cotton rolls, non-latex rubber dam, topical benzocaine, dental mirror, glass ionomer dispensing gun, dental explorer, triturator for the glass ionomer, cotton gauze, suction tip, air-water syringe.

Interventions

rubber dam or cotton roll isolation

DEVICEFuji Triage

glass ionomer sealant

Sponsors

Louisiana State University Health Sciences Center in New Orleans
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

The evaluator will not have knowledge of which type of isolation was used when placing the sealants.

Intervention model description

each patient is serving as their own control

Eligibility

Sex/Gender
ALL
Age
5 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

healthy children who need sealants on 4 permanent molars that are not hypo plastic, are caries-free, and with no enamel defects. \-

Exclusion criteria

hypoplastic molars, caries, teeth with existing restorations, and those with enamel defects, \-

Design outcomes

Primary

MeasureTime frameDescription
retention rate of sealants6 monthsretention rate for sealants placed with different modes of isolation

Contacts

Primary ContactSuzanne E Fournier, DDS
sfour1@lsuhsc.edu504-941-8199
Backup ContactDaniel Kim, 'DMD
dkim5@lsuhsc.edu504-941-8199

Outcome results

None listed

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