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Sealant: 10-years Clinical Trial of Sealed of Margin Failures

Sponsor
University of Chile (Other)
Overall Status
Completed
CT.gov ID
NCT02075801
Collaborator
(none)
32
Enrollment
1
Location
126.1
Duration (Months)
0.3
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

  • Assess the effectiveness of sealing localized marginal defects of amalgam restorations that were initially scheduled for replacement of restorations.

  • The hypothesis was that sealed defective margins of the amalgam restorations shows similar performance than replacement amalgam restorations.

Condition or Disease Intervention/Treatment Phase
  • Other: Sealing of amalgam margin defects
  • Other: Sealing of amalgam margin defects

Detailed Description

Study Design

Were examined 157 patients with 586 amalgam restorations that were recruited at the Operative Dentistry Clinic, at the Dental School, University of Chile with the indication of amalgam replacements, of them, a cohort of thirty two patients (19 females and 13 males, mean age = 27 years old), with 73 Class I amalgam restorations, that presented one or more localized margin defects (Bravo or Charlie according to modified United State Public Health Service, USPHS criteria), were included in the study. The protocol was approved by the Institutional Research Ethics Committee of the Dental School at the University of Chile, Investigation Project, School of Dentistry (0205) and all patients signed the informed consent form and completed the registration form. Only Faculty members were accepted to provide the treatment.

Treatment Groups Criteria: 73 restorations with defective margins were evaluated in accordance with the modified USPHS criteria and assigned to either the sealant (n=26), repair (n=21) and control groups (n=26).

Restorations Assessment: The quality of the restorations were evaluated using the modified U.S. Public Health System/Ryge criteria. Two examiners assessed the restorations independently and by visual and tactile (mouth mirror number 5) examination using an explorer (N° 23) and indirectly by radiographic, examination, for interproximal observation (Bite Wing). All the restorations were examined at baseline and each year during four and ten years after treatment. The restorations assessment was carried out by five parameters: marginal adaptation (MA), roughness (R), secondary caries (SC), marginal stain (MS) and teeth sensitivity (TS). If any difference was recorded between the 2 independent examiners, and they did not reach an agreement, a third clinician was called to assist with the process decision. If the three clinicians they did not reach an agreement, the lower score was recorded. All three clinicians participated in calibration exercises at the beginning and before the last examination took place and the inter-examiner reliability results were Kappa=0.74 at the baseline and Kappa=0.87 at the ten year.

A change from Bravo to Alpha was considered an improvement and a change from Alpha to Bravo was considered downgrade.

Caries risk assessment: A graphical computed program (CARIOGRAM) was used for individual´s patients caries risk assessed, the program weighted the interaction between the following 10 caries related factors: Caries experience, related general disease, diet contents, diet frequency, plaque amount by Silness Löe Index, semi quantitative detection of mutans streptococci and lactobacilli in saliva by Caries Risk Test (CRT), fluoride program, amount of saliva stimulated secretion by CRT Buffer (Vivadent), saliva buffer capacity and clinical judgment. Patients were classifying in high, intermediate and low caries risk. Additionally the results also indicate where targeted actions to improve the situation will have the best effect.

Patients were recalled ten years after the treatment, for clinical assessment by the same examiners, applying the same criteria used at baseline. Failed restorations were removed from the study and treated according to the diagnosed needs.

Statistical analysis The ordinal dependent variable was changed in level of the modified USPHS criteria from the baseline value. The assigned score of each restoration reflected the worst result for any of the parameters. The results of each group in terms of degradation or upgrade were analyzed by Friedman range non-parametric test to compare the pre and postoperative conditions. Additionally, the performance of all groups was contrasted using the Mann Whitney test to determine the differences between the upgrade and downgrade of the restoration´s quality. The statistical significance was set at 95%, α=0.05 and β=0.80 for statistical analysis.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
32 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Longitudinal Results of a 10-years Clinical Trial of Sealed Margin Failures of Amalgam Restorations
Study Start Date :
Aug 1, 2003
Actual Primary Completion Date :
Feb 1, 2014
Actual Study Completion Date :
Feb 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Defective amalgam restorations

Treatment Groups: A. Sealing of amalgam margin defects: Defective areas were acid etched with 35% phosphoric acid for 15 seconds. A resin-based sealant (Sealant, 3MESPE)was applied over the defective area. The sealant was polymerized with a photo curing unit (Curing-Light 2500, 3MESPE) for 40 seconds. Rubber dam isolation was used for this procedure. All treatments were applied by the same clinician. B. Replacement Group: The clinician totally removed and replaces the defective restoration with a new amalgam (Tytin, Kerr, Orange, USA). Rubber dam isolation was used for this procedure. All treatments were applied by the same clinician. C. Control Group: The defective restorations did not receive any treatment.

Other: Sealing of amalgam margin defects
Comparison between sealing of amalgam margins defects, replacement and non treated groups.

Other: Sealing of amalgam margin defects
A.Sealing of amalgam margin defects: were acid etched with 35% phosphoric acid for 15 seconds. A resin-based sealant (Clinpro Sealant, 3MESPE) was applied over the defective area. The sealant was polymerized with a photocuring unit (Curing Light 2500, 3M ESPE) for 40 seconds. Rubber dam isolation was used for this procedure. All treatments were applied by the same clinician. B.Replacement Group: The clinician totally removed and replaces the defective restoration with a new amalgam (Tytin, Kerr Corporation, Orange, CA, USA). Rubber dam isolation was used for this procedure. All treatments were applied by the same clinician. C.Control Group: The defective restorations did not receive any treatment.
Other Names:
  • Use of Selant to seal amalgam margins defects

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Changes of Amalgam restorations quality according to United Stated Public Health Service (USPHS) [Baseline and 10 after treatment]

      Restorations Assessment: The quality of the restorations were evaluated using the modified U.S. Public Health System criteria. Two examiners assessed the restorations independently and by visual and tactile examination. All the restorations were examined at baseline and ten years after treatment. The restorations assessment was carried out by five parameters: marginal adaptation, roughness, secondary caries, marginal stain and teeth sensitivity. All three clinicians participated in calibration exercises at the beginning and before the last examination took place and the inter-examiner reliability results were Kappa=0.74 at the baseline and Kappa=0.87 at the ten year.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion criteria:

    • Patients with amalgam restorations with marginal deficiencies that were judged to be suitable for sealing.

    • Older than 18 years of age ¨

    • More than 20 teeth in their mouth

    • The restorations had to be in functional occlusion with an opposing natural tooth

    • With at least one proximal contact area with and adjacent tooth

    • Area out of the restoration´s failures in good condition

    • Patients who agree and sign the informed consent for participating in the study.

    Exclusion Criteria:

    • Patients with contraindications for regular dental treatment based on their medical history

    • Special aesthetic requirements that could not be solved by this alternative treatment

    • Xerostomia or who were taking medication that significantly decreased salivary flow

    • High caries risk

    • Psychiatric or physical diseases, that interfered with teeth hygiene.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Chile Santiago Region Metropolitana Chile

    Sponsors and Collaborators

    • University of Chile

    Investigators

    • Principal Investigator: Gustavo Moncada, DDS, University of Chile

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Gustavo Moncada, Main Investigator, University of Chile
    ClinicalTrials.gov Identifier:
    NCT02075801
    Other Study ID Numbers:
    • PRI-ODO-0207
    First Posted:
    Mar 3, 2014
    Last Update Posted:
    Mar 3, 2014
    Last Verified:
    Feb 1, 2014
    Keywords provided by Gustavo Moncada, Main Investigator, University of Chile
    Sealant, Margins Defect, Amalgam
    Additional relevant MeSH terms:
    Dental Caries

    Study Results

    No Results Posted as of Mar 3, 2014