Tooth Wear:m Tooth Wear : Diagnosis- Treatment Decision

Dental Wear Clinical Trial

Official title:

Tooth Wear : Diagnosis- Treatment Decision- Management- Monitoring- Randomized Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03540264
• Other study ID #: 2017/24NOV/531
• Status: Recruiting
• Phase: N/A
• Start date: February 26, 2018
• Est. completion date: December 31, 2020

Study information

• Verified date: March 2019
• Source: Cliniques universitaires Saint-Luc- Université Catholique de Louvain
• Contact: DE CARVALHO Joana, Dentist, Pr
• Phone: 0032 2 764
• Email: joana.carvalho[@]uclouvain.be
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Tooth wear is a physiological process occurring from normal functioning of the dentition throughout lifetime.

Description:

The studies in the current literature indicated that both techniques of tooth preparation and the materials used are appropriate for the treatment of this condition, but the tendency is to reduce tooth preparation as reasonably possible. In this clinical trial, the investigators will compare the outcomes of direct resin composite and indirect polymer-infiltrated-ceramic-network.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 52
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients aged 18 years or older, in good general health, willing to participate in the study and accepting to come to regular controls in the future.

• Patients representing any type of significant tooth wear (= 1 mm depth) with dentine exposure in at least 4 teeth: localized tooth wear anterior or posterior teeth and generalized tooth wear anterio and posterior teeth.

• Patients having posterior support with at least 4 molars in occlusion, 1 pair per side, excluding third molar.

Exclusion Criteria:

• Patients wearing removable partial prosthesis

• Patients presenting skeletal Cl III occlusal Relationship

• Patients with remaining clinical crown of = 3 mm in height and presenting tooth anomaly in shape and number in addition to anterior diastemas.

• Patients with symptomatic temporomandibular joint disorders.

Related Conditions & MeSH terms

• Dental Wear
• Tooth Wear

Intervention

Device:
• Clearfil Majesty TM
Tooth wear - composite resin
• Vita-Enamic®
Tooth wear - polymer-infiltrated-ceramic-network

Locations

Country	Name	City	State
Belgium	Cliniques Universitaires Saint-Luc	Brussel

Sponsors (1)

Lead Sponsor	Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Restoration	by modified USPHS criteria	up to 3 years