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Two-Year Clinical Comparison of Three Different Restorative Materials in Class II Cavities

Two-Year Clinical Comparison of Three Different Restorative Materials in Class II Cavities

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190405001
Enrollment
Unknown
Registered
2019-04-05
Start date
2016-11-01
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

Healthy persons between the age group of 20 and 32 years.

Interventions

Charisma Smart Composite group: Single Bond Universal adhesive (3M ESPE&#44
Neuss&#44
Germany) was applied to the cavities according to the manufacturer’s instructions and polymerized with an LED light device (Valo&#44
1000 mW / cm2&#44
Utah&#44
USA) for 10 s. Charisma Smart Composite (CSC) was placed incrementally by using horizontal increments&#44
not exceeding 2 mm in the cavity&#44
and each layer was cured for 20 s. After removal of the matrix and wedges&#44
the restorations were additionally cured for 10 s from the buccal and palatal/lingual sides.,Filtek Bulk Fill Posterior Restorative group: Single Bond Universal adhesive was applied and polymerized as
but at no more than 4 mm thick&#44
and was cured for 20 s. After removal of the matrix and wedges&#44
the restorations were additionally cured for 10 s from the buccal and palatal/lingual sides.,Equia Forte Fil group: Cavity Conditioner (GC) was applied to the cavities for 10 s&#44
washed&#44
and gently dried. After isolation&#44
an Equia Forte Fil (EF) capsule was placed in an automatic mixer and stirred for 10 s. The capsule was then placed in a special applicator and injected into the cavities. After the manufacturer’s re
the restoration was finished&#44
polished and gently dried. Equia Forte Coat (GC) was applied to the restoration surfaces and cured for 20 s.
Experimental Other,Experimental Other,Experimental Other
conventional composite resin,buklfill composite resin,high viscosity glass ionomer

Sponsors

Erciyes University Scientific Research Projects Foundation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 32 Years

Inclusion criteria

Inclusion criteria: 1) the patient has no systemic disease 2) the patient should be over 18 years of age; 3) the patient should have good periodontal status; 4) teeth to be restored should be vital; 5) teeth to be restored should have proximal contacts on both mesial and distal surfaces and be in occlusion with the antagonist teeth 6) teeth that have class II caries lesions in external and middle 1/3 of dentine thickness as determined radiographically

Exclusion criteria

Exclusion criteria: 1) the existence of xerostomia and bruxism; 2) absence of adjacent and antagonist teeth; 3) extremely poor oral hygiene, severe or chronic periodontitis; 4) pregnant or lactating women; 5) teeth that have any restoration, endodontic treatment, periodontal and periapical pathology 6) the patients who are undergoing orthodontic treatment.

Design outcomes

Primary

MeasureTime frame
Clinical evaluation 2 year USPHS criteria

Secondary

MeasureTime frame
Radiographic evaluation 2 year bite-wing radiographies

Countries

Türkiye

Contacts

Public ContactHacer Balkaya

Faculty of Dentistry, Erciyes University,

dhacer89@hotmail.com+905050187028

Outcome results

None listed

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