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Contact Tightness of Zirconomer Versus Nanohybrid Composite in Occlusoproximal Cavities in Molars

Comparison of Proximal Contact Tightness of Zirconia Reinforced Glass Ionomer Versus Conventional Nanohybrid Resin Composite: a Randomized Clinical Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06596707
Enrollment
52
Registered
2024-09-19
Start date
2023-07-12
Completion date
2024-11-01
Last updated
2024-09-19

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

Conditions

Contact Tightness in Restoring Proximal Surfaces in Posterior Teeth

Keywords

Zirconomer, Glass Ionomer, Contact tightness, Occlusoproximal cavities, Resin composite, Class II

Brief summary

To achieve an optimal contact area is essential to avoid tooth migration, food impaction, and the occurrence of secondary caries. However, proximal restorations constitute challenge for the professional and tight contact points are difficult to obtain depending not only on tools used, but also on type of restorative material. Current tooth-colored restorative materials are not condensable and there is shrinkage with setting. The aim of this study is to compare the proximal contact tightness of zirconia reinforced glass ionomer versus conventional nanohybrid resin composite when used in class II cavities.

Interventions

PROCEDUREZirconomer

zirconia modified glass ionomer

PROCEDURENanohybrid composite

conventional composite

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
19 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Eligibility Criteria of participants: Inclusion Criteria of participants: * Patients with occlusoproximal caries in molars classified as ICDAS III or IV. * 19-35 years. * Males or Females. * Co-operative patients approving to participate in the trial.

Exclusion criteria

of participants: * Pregnancy. * Disabilities. * Systemic disease or severe medical complications. * Allergic history concerning methacrylate. * Rampant caries. * Heavy smoking. * Xerostomia. * Lack of compliance. * Evidence of severe bruxism, clenching, or temporomandibular joint disorders. b- Eligibility Criteria of teeth: Inclusion Criteria of teeth: * Occlusoproximal caries in molars classified as ICDAS III or IV. * Vital upper or lower posterior teeth with no signs of irreversible pulpitis. * Intact contact with opposing teeth. * Teeth with no previous restorations in other surfaces.

Design outcomes

Primary

MeasureTime frameDescription
Contact Tightnessbaseline, 3 months, 6 months, 9 months and 1 yearMeasuring the adequacy of proximal contact restoration using intervention ' zirconomer" versus control which is Nanohybrid resin composite. Heaviness of this contact using Modified USPHS criteria. USPHS criteria are standardized in which a dental floss is used. Contact tightness can have one of three scores: Alpha Bravo Charlie

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026