Skip to content

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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201906600044618
Enrollment
82
Registered
2019-06-12
Start date
2019-09-02
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral Health

Interventions

FILTEK SUPREME ULTRA RESTORATIVE

Sponsors

IKEM OBEHI MARY
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Comparing the clinical and radiological outcome of a bioactive ionic resin with a nano-hybrid composite restoration.

Secondary

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

Countries

Nigeria

Contacts

Public ContactOBEHI IKEM

SENIOR RESIDENT

obehi.ikem@gmail.com+2348166804118

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026