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Evaluation of Two Different Methods of Resin Composite Application In Class II Restorations

2 oktober 2015 bijgewerkt door: Damascus University

Evaluation of Two Different Methods of Resin Composite Application Using Bulk-fill Technique In Class II Restorations

Three clinical groups will be evaluated. Each group of patients will undergo one method of Resin Composite application (multi-layer technique 'control group' - bulk-fill Technique - Sonicfill technique). The restored teeth will be followed-up till one year. A comparison is going to be made between the three groups in relation to the modified United Sates Public Health Service (USPHS) criteria of good restorations.

Studie Overzicht

Toestand

Voltooid

Conditie

Interventie / Behandeling

Gedetailleerde beschrijving

The modified USPHS criteria include the evaluation of seven characteristics of the restorations: color match, marginal integrity, surface texture, wear of both restoration and antagonist, recurrent dental caries, fracture or detachment, and gingivitis around the abutment.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

60

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

  • Syrische Arabische Republiek
      • Damascus, Syrische Arabische Republiek, DM20AM18
        • Department of Operative Dentistry, University of Damascus Dental School

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

15 jaar tot 60 jaar (Kind, Volwassen)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  1. Cooperated patients.
  2. Good general health.
  3. Good oral hygiene.
  4. Aged 15 to 60 years.
  5. Class II restoration (upper or lower)
  6. Full erupted teeth.
  7. Caries value D3 -D4 according to Daignodent.

Exclusion Criteria:

  1. If the caries value according to Daignodent is less than D3 -D4.
  2. If the tooth is partially erupted.
  3. Class II box-like cavity only without any extensions.
  4. Patient outside the required age range (15-60 years).
  5. Bad oral hygiene.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Geen tussenkomst: Conventional Technique
Multi-layer filling technique
Actieve vergelijker: Bulk fill technique
Procedure: Bulk fill
This is one of the composite restoration application techniques
Experimenteel: SonicFill technique
Procedure: SonicFill
This is the recent intervention under evaluation

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Color Match
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Color match

  1. The restoration appears to match the shade and translucency of adjacent tooth tissues.
  2. The restoration does not match the shade and translucency of adjacent tooth tissues, but the mismatch is within the range of tooth shade.
  3. The restoration does not match the shade and translucency of adjacent tooth tissues, and the mismatch is outside the normal range of tooth shade and translucency.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
Change in Marginal Integrity
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Marginal integrity

  1. The explorer does not catch when drawn across the surface of the restoration toward the tooth, or, if the explorer does catch, there is no visible crevice along the periphery of the restoration.
  2. The explorer catches and there is visible evidence of crevice, into which the explorer penetrates, indicating that the edge of the restoration does not adapt closely to the tooth structure.
  3. the explorer penetrates a crevice defect.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
Change in Surface Texture
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Surface texture:

  1. Surface texture is similar to polished enamel as determined by means of a sharp explorer.
  2. Surface texture is gritty similar to a surface subject to a white stone or similar to a composite containing supramicron sizes particles.
  3. Surface pitting is sufficiently coarse to inhibit the continuous movement of an explorer across the surface.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
Change in Restoration Wear
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Wear

  1. The restoration is continuation of existing anatomic form or is slightly flattened.
  2. A surface concavity is evident.
  3. There is a loss of restorative substance such that a surface concavity is evident. Replacement or restorative treatment is required.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
Recurrent dental caries
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Recurrent dental caries:

  1. The restoration is a continuation of existing anatomic form adjacent to the restoration.
  2. There is visual evidence of dark deep discoloration adjacent to the restoration.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
The Fracture/detachment Status
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Fracture/detachment:

  1. No bulk fracture/detachment is present.
  2. Bulk fracture/ detachment is evident.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.
Change in gingival status
Tijdsspanne: Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Gingival status

  1. No clinical inflammation is present.
  2. Clinical inflammation is present.
Assessment will be done at (T0) within the first hour following composite sitting, (T1) after 3 months, (T2) after six months, (T3) after six months, (T4) at 12 months following application.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Damascus University

Onderzoekers

  • Hoofdonderzoeker: Rahaf Alkurdi, DDS MSc, PhD student, Department of Operative Dentistry, University of Damascus Dental School, Damascus
  • Studie directeur: Souad Abboud, DDS MSc PhD, Associate Professor, Operative Dentistry Department, University of Damascus Dental School, Damascus

Publicaties en nuttige links

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Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 juli 2014

Primaire voltooiing (Werkelijk)

1 juli 2015

Studie voltooiing (Werkelijk)

1 oktober 2015

Studieregistratiedata

Eerst ingediend

4 juli 2014

Eerst ingediend dat voldeed aan de QC-criteria

4 juli 2014

Eerst geplaatst (Schatting)

9 juli 2014

Updates van studierecords

Laatste update geplaatst (Schatting)

5 oktober 2015

Laatste update ingediend die voldeed aan QC-criteria

2 oktober 2015

Laatst geverifieerd

1 oktober 2015

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Andere studie-ID-nummers

  • UDDS-OperDent-01-2014

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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