Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Comparison of Proximal Contacts and Contours in Class II Composite Restoration With Pre-cured Composite Inserts Versus Contact Making Instrument Technique. A Randomized Control Clinical Trial.

18 maggio 2022 aggiornato da: Foundation University Islamabad

The objective of this randomized control cinical trial will be to compare the effectiveness of precured composite inserts in obtaining tight and adequate conatacts in class 2 restorations when compared with the contact making instrument technique among patients treated at the operative depatment of Foundation Umiversity College of Dentistry.

This is a single centre based randomized control clinical trial in which intervention arm 1 will get there class 2 restoration done with precured composite inserts and interention arm 2 will recieve treatment with contact making instrument technique. The control arm will recieve restoration using the conventional composite layering technique.

Panoramica dello studio

Descrizione dettagliata

Study design : randomized control clinical trial with three intervention arms

Study setting : operative department , foundation university college of dentistry Islamabad Pakistan.

Sample size : the sample size was calculated using the NCSS PASS software. A total od 180 patients will be tested in the study divided in three groups of 60 patients each. Consent will be taken from pateints on a standardized form approved by the ethics review committe in the operatory where the initial assessment will be done.

Procedure:

  1. number of operaters will be restricted two, with similar level of experience in order to minimize operater variation
  2. the investigator and co investigator will calibrate each other on the sequence of the procedure and assessment to enhance standardization of procedure
  3. local anaesthesia will be given to patients using lidocaine 2% solution available for dental use in 1.8 ml carpule
  4. rubber dam will used for isolation and moisture control in the working field.
  5. the tooth to be restored will be seperated from the adjacent tooth using wooden wedges.this will allow seperation of teeth.
  6. cavity preparation will be done using a high speed handpiece(W&H) with a round bur(prima) (no1/6 or 1/4). After initial penetration through enamel the carious lesion will be excavated using a a carbide bur in a slow speed handpiece.

    after caries removal any unsupported enamel at the gingival floor will be removed using a gingival margin trimmer.

    the cavity shape will be finalized using a pear shaped bur(243).

  7. the width of the final cavity will be measured using a perio probe from the buccal or labial cavo surface margin. Only cavities with less than 1/2 the width of the distance or less from the buccal or lingual cusp tip will be included in the study.
  8. sectional metal matrix (unimatrix by TDV Brazil,1/4" by 0.0015,1/4" by.002,height and thickness of matrix) will be applied after removing the previously placed wooden wedges. The wedges will be reintroduced after sectional matrix application.
  9. the cavity will be etched using 37% phosphoric acid etchant(30 seconds enamel and 15 seconds dentine) followed by rinsing for 30 seconds with the triple syringe. the cavity will be gently air dried while keep a dried cotton pellet in the cavity to absorb excess moisure for 30 to 45 seconds.Prime and Bond NT (Dentsply) adhesive will be applied to the cavity followed by curing for 20 seconds with an led based curing light (O-light,DTE wavelength of 400nm visible blue light). The cavities in all intervention arms will be restored with neo spectre NT composite(dentsply). (the detail of each intervention arm is given under their respective headings)
  10. after the cavities are filled the matrix band and the wedges will be removed.the cavity will be finished using diamond burs and composite finishing spirals(azdent). occlusal adjustment will be done where needed using articulating paper.
  11. the final restoration will be polished using diamond polishing paste(ultradent) and goat hair brushes (ultradent)

Assessment

  1. assessment will be done by passing waxed dental floss between the filling and adjacent tooth by a single independent assessor blinded to the treatment allocation.
  2. outcome will be assessed using the contact tightness and contour component of the modified USPHS rating scale
  3. data collection will be done at the end of the treatment using a printed porforma for recording the study variables.

Data analysis

  1. will be done using spss 26
  2. for continouse variables like age and cavity wifth and depth , mean and standard deviations will be computed.

    comparison of these variable will be done by one way anova test

  3. for categorical variables like gender, type of tooth,location of cavity,contact tightness and contour(outcome variables) frequencies in percentages will be reported. these variables will be compared using kruskal-wallis test at 0.05 level of significance

Tipo di studio

Interventistico

Iscrizione (Anticipato)

180

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 12 anni a 55 anni (Bambino, Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion criteria

  1. patient requiring treatment for class 2 cavity
  2. patient age 12 to 55 years
  3. Maxillary and Mandibular first and second premolar
  4. Maxillary and Mandibular first and second molar
  5. Maximum occlusal cavo surface width of 2/3rd of intercuspal width
  6. Cavity depth upto 3/4th of occlusocervical length measured from diagnostic radiograph
  7. Teeth with adjacent fully erupted teeth adjacent to a cavity side Exclusion criteria

1)Mentally and physically handicapped patient 2)Pregnant females 3)Patients with naturally spaced teeth 4)Patients with moderate or advanced periodontitis 5)Endodontically treated teeth 6)Teeth with excessive occlusal wear and erosion of teeth 7)Tooth adjacent to cavity side is missing 8)Teeth with orhtodontic bands and brackets 9)Tooth adjacent to cavity side is restored

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Precure composite insert technique
After curing of bonding agent a 2mm increment of composite will be placed on the gingival floor of the cavity and cured. a measured volume of composite(3mm height and 2mm width) will be cured outside the oral cavity on a flat plastic instrument for 40 seconds. a second increment of composite will be placed on the cavity and the precured composite will be pressed in the uncured increment and pressed outward against the matrix band and light cured for 20 seconds the rest of the cavity will be filled using the oblique layering technique.
After curing of bonding agent a 2mm increment of composite will be placed on the gingival floor of the cavity and cured. a measured volume of composite(3mm height and 2mm width) will be cured outside the oral cavity on a flat plastic instrument for 40 seconds. a second increment of composite will be placed on the cavity and the precured composite will be pressed in the uncured increment and pressed outward against the matrix band and light cured for 20 seconds the rest of the cavity will be filled using the oblique layering technique.
Sperimentale: Contact Making Instrument

a 1-2mm increment of the composite will be placed in the gingival floor of the proxial box.

a contact forming instrument will be placed in this uncured increment and an outward force will be applied using the instrument from the inside of the matrix band. The composite will then be cured for 20 seconds to achieve a tight contact.

a 1-2mm increment of the composite will be placed in the gingival floor of the proxial box.

a contact forming instrument will be placed in this uncured increment and an outward force will be applied using the instrument from the inside of the matrix band. The composite will then be cured for 20 seconds to achieve a tight contact.

Comparatore attivo: Incremental composite layering technique
Increments will be placed in 1-2mm increments in oblique layering manner by a flat plastic instrument and condenser .Each increment will be cured for 20 seconds till the cavity is slightly overfilled.
Increments will be placed in 1-2mm increments in oblique layering manner by a flat plastic instrument and condenser .Each increment will be cured for 20 seconds till the cavity is slightly overfilled.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Contact tightness and Contour of Class 2 composite restoration
Lasso di tempo: 1 day
The contact tightness and contour of the filling will be assessed using the modified united states public health service system rating scale which has is used in studies on dental materials.
1 day

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Anticipato)

1 dicembre 2022

Completamento primario (Anticipato)

30 marzo 2023

Completamento dello studio (Anticipato)

31 marzo 2024

Date di iscrizione allo studio

Primo inviato

18 maggio 2022

Primo inviato che soddisfa i criteri di controllo qualità

18 maggio 2022

Primo Inserito (Effettivo)

23 maggio 2022

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

23 maggio 2022

Ultimo aggiornamento inviato che soddisfa i criteri QC

18 maggio 2022

Ultimo verificato

1 maggio 2022

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • FUI/CTR/2022/7

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi