ONE-YEAR CLINICAL AND RADIOLOGIC OUTCOME OF A BIOACTIVE IONIC RESIN VERSUS NANO-HYBRID COMPOSITE RESTORATION ON CARIOUS POSTERIOR TEETH.

Not Applicable

• Conditions: Oral Health

• Registration Number: PACTR201906600044618
• Lead Sponsor: IKEM OBEHI MARY

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-06-11
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 82

Inclusion Criteria

1. Subjects with at least 2 clinically detectable proximo-occlusal or proximal cavities involving any posterior permanent teeth, with each tooth in the same arch or opposing arch.
2. Moderate cavities according to the International Caries Classification & Management System (ICCMS)333 after plaque removal for an appropriate visual examination of the tooth surfaces by means of prophylactic paste and brush, with appropriate light and the use of a ball-end probe (WHO probe) according to ICDAS examination protocol.69
3.Carious teeth with radiographic evidence of no periodontal or pulpal involvement.
4.Carious teeth should be devoid of pain suggestive of irreversible pulpitis.
5.Subjects who give verbal and signed consent to take part in the study.

Exclusion Criteria

i. Subjects with tooth wear.
ii.Subjects with parafunctional habits.
iii.Subjects with carious teeth lacking opposing and/or abutting standing teeth.
iv.Subjects with poor oral hygiene score of greater than 3.0 according to Greene and Vermillion.335
v.Fractured or cracked tooth

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comparing the clinical and radiological outcome of a bioactive ionic resin with a nano-hybrid composite restoration.

Secondary Outcome Measures

Name	Time	Method
1. To determine one-year radiological outcome of ACTIVA™ BioACTIVE restorative material.<br>2. To determine the level of surface and marginal staining of ACTIVA™ BioACTIVE restorative material at 12-months after restoration<br>3. To determine the marginal adaptation of ACTIVA™ BioACTIVE restorative material at 12-months after the restoration. <br>4. To determine the one-year survival rate of ACTIVA™ BioACTIVE restorative material.<br>