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152012023

Digital crowns versus prefabricated crowns on primary teeth
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT06305845
digital crowns
zirconia crowns
primary teeth
Source : Importé depuis le centre
Recrutement fermé
Dernière modification : 2024/05/30

Population cible

Condition médicale (spécialité visée)

Donnée non disponible

Profil des participants

Sexe(s) des participants

ALL

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Inclusion Criteria:

* Patients within the age group of 4-10years. Badly decayed or multi-surface affected primary teeth Healthy children free of any systemic disease Patients with cooperative behavior rating definitely positive or positive on the Frank rating scale

Exclusion Criteria:

* Teeth with developmental disturbances
* Teeth with poor prognosis as signs of necrosis, extensive pathological root resorption
* patients with parafunctional habits

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Digital crowns
État du recrutement
unknown
Zirconia crowns
État du recrutement
unknown
Données à jour depuis : 30 mai 2024

Description de l'étude

Résumé de l'étude

Badly decayed primary molars will be treated by performing the pulp therapy technique indicated, then the patients will be randomized into two groups to receive the restorative intervention. For the intervention group, teeth will be prepared to receive the digital crown after intraoral scanning while for the control group, teeth will be prepared to receive the prefabricated zirconia crowns. Teeth will be followed up clinically for 1 year, at 1, 6 and 12 months.

Source : Importé depuis le centre

This is a 12-month randomized, controlled, two parallel arms clinical trial. Patients aging from 4 to 10 years with multi-surface decay will be selected. After caries removal and pulp exposure, pulpotomy or partial pulpectomy technique will be performed,then the teeth will be randomized to the interventional group of digital crowns or to the control group of prefabricated zirconia crowns. For preparation of digital crowns, the occlusal reduction was done by 1.5-2 mm. The proximal contacts will be broken and the entire clinical crown structure was reduced by 0.8-1.0 mm , followed by a a subgingival finish line . For the scanning procedure, the upper and lower arches will be scanned with intra oral scanner, and making sure every point is well detailed . A third scan of the occlusal bite is then performed in order to establish the patient's occlusion.

For the milling procedure, Brilliant Crios composite the blocks will be used and milled with the CEREC MC X milling unit . The inner surface of the crown will be sandblasted with Al2O3 .

For zirconia crown preparation, occlusal reduction of 1.5-2mm will be performed by a football diamond bur. The occlusal third of the buccal and lingual surfaces will be also reduced . The whole crown will be reduced by 0.8-1.0 mm by means of a tapered diamond stone .A shoulder finish line will be created. The try in crown will be tested, then the shoulder finish line will be removed and the preparation will be extended subgingivally to feather-edge.

The crowns will then be cemented with the self-adhesive resin cement (Solocem, Coltene, Whaledent, Altstatten, Switzerland) .Light curing was performed while applying pressure on the crown and then waiting for 5 minutes for complete cementing

Source : Importé depuis le centre

Sites

Centres participants

    1 centres
  • NATIONAL RESEARCH CENTRE

    Cairo

    EGYPT

    Recrutement local
    État du recrutement: FERMÉ

Dernière modification : 30 mai 2024
Données à jour depuis : 2 juin
Origine des données : clinicaltrials.gov
Référence clinicaltrials.gov: NCT06305845