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Comparing Three Dental Techniques to Improve Fillings in Back Teeth.

TO COMPARE AND EVALUATE THE FUNCTIONAL PROPERTIES OF CLASS 2 COMPOSITE RESTORATIONS USING THREE DIFFERENT MATRIX SYSTEMS AN IN VIVO STUDY - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105365
Enrollment
30
Registered
2026-03-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: K029- Dental caries, unspecified Health Condition 2: K029- Dental caries, unspecified

Interventions

Intervention1: CLASS 2 COMPOSITE RESTORATIONS: CLASS 2 COMPOSITE RESTORATIONS DONE USING 3 DIFFERENT MATRIX SYSTEMS Control Intervention1: CLASS 2 COMPOSITE RESTORATIONS: CLASS 2 COMPOSITE RESTORATION

Sponsors

ASHIBA K
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with proximal Class II carious lesions (MO or DO) in posterior maxillary or mandibular teeth. Teeth indicated for direct composite restoration. Teeth with vital pulp showing no clinical or radiographic signs of irreversible pulpitis. Teeth with normal response to pulp sensibility testing using an electric pulp tester (EPT). Teeth with adequate remaining tooth structure to allow conservative Class II cavity preparation. Patients willing to participate in the study and who provided written informed consent. Patients able to tolerate rubber dam isolation and routine restorative procedures.

Exclusion criteria

Exclusion criteria: Teeth with signs or symptoms of irreversible pulpitis or pulpal necrosis (spontaneous pain, lingering pain, no response to EPT). Teeth with periapical pathology evident on radiographic examination. Teeth with extensive carious destruction requiring indirect restorations (inlays, onlays, or crowns). Previously restored teeth with proximal restorations in the same surface. Teeth with cracks, fractures, developmental defects, or structural anomalies. Patients with poor oral hygiene or high caries risk that could compromise restoration longevity. Patients with parafunctional habits such as bruxism or clenching. Patients with known allergy or hypersensitivity to resin-based dental materials. Medically compromised patients or those with systemic conditions contraindicating routine dental treatment. Pregnant or lactating women (if radiographic exposure was considered).

Design outcomes

Primary

MeasureTime frame
Primary Outcome Measures - Fracture of material and retention (F1) - Determined through visual and radiographic examination. - Scored using the FDI scale (1 5). - Marginal adaptation (F2) - Evaluated visually and with a metric probe. - Scored using the FDI scale (1 5). - Proximal contact point (F3) - Assessed using metal blades (0.025 0.1 mm) and dental floss. - Scored using the FDI scale (1 5). - Form and contour (F4) - Evaluated visually and radiographically. - Scored using the FDI scale (1 5). Timepoint: at the time of treatment

Secondary

MeasureTime frame
patient factor operative efficiency radiographic factorsTimepoint: at the time of treatment

Countries

India

Contacts

Public ContactASHIBA K

VYDEHI INSTITUTE OF DENTAL SCIENCES AND RESEARCH INSTITUTE

ashiba.k123@gmail.com9567451886

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026