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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04738604
Other study ID # 91120
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date February 1, 2023

Study information

Verified date August 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

in patients with Class I Cavities, will the use of Zenit Nano Ceramic Composite restorations have similar clinical performance to conventional Ceram-X Nano Ceramic Composite restorations, evaluation of restorations will be done at baseline, six, and twelve months using Modified USPHS Ryge criteria.


Description:

The study will be conducted in the clinic of Conservative Dentistry Department, Faculty of Dentistry, Cairo University; the operator in charge samah mohamed bahig, The subjects fulfilling the eligibility criteria of the trial will be selected from the regular attendees at the clinic of Conservative Dentistry Department, Faculty of Dentistry, Cairo University. Patient examination will be done including medical history, dental history, extra-oral examination and intraoral examination. A periapical radiograph will be taken prior to restorative procedures to assess the degree of approximation of caries to pulp, intactness of lamina dura and/or presence of any periapical radiolucency to exclude the case. The field of operation will be isolated with the application of a rubber dam if possible. Otherwise, cotton rolls and the saliva ejector will be used for moisture control. For cavity preparation, local anesthetic (MepecaineL, Alexandria Company, Egypt) solution will be administrated to control patient discomfort during the procedure. The cavities will be prepared by using cylindrical #314 (Komet®, Germany) in a high speed handpiece (Sirona, Germany) rotating at high speed with copious coolant. Remaining soft caries -if present- will be removed using sharp excavator (Maillefer, Dentsuply, Switzerland).After the cavity preparation is finished, it will be thoroughly air-water cleaned. The bonding system; the Prime and Bond universal adhesive (Dentsply De Trey GmbH, Konstanz, Germany) will be applied according to the following instructions recommended by the manufacturer and rubbed for 20 seconds then blown with a gentle air blow for 5 seconds to evaporate the solvent and then light curing for 10 seconds using LED light curing unit (>700 mW/cm2).The prepared cavities will be restored with Zenit Nano Ceramic Composite (PRESIDENT DENTAL, GmbH, Munich, Germany) will be applied with incremental placement technique (maximum: 2-mm layer). Increments will be light curing for 40 seconds according to manufacturer's instructions. and for the control group cavities will be restored withCeram•X (Dentsply De Trey GmbH, Konstanz, Germany) with incremental placement technique (maximum: 2-mm layer). Increments will be light cured for 20 seconds according to manufacturer's instructions.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 28
Est. completion date February 1, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 54 Years
Eligibility Inclusion Criteria: - • Male or female gender. - Only co-operative patients approving to participate in the trial. - Good oral hygiene. - Medically free adult patients. - The age range of the patients is 20 to 54 years - Vital first and second molars, with Class I lesion. - Functioning tooth with presence of an opposing. - Healthy periodontium Exclusion Criteria: - Patients with disabilities. - Patients having systemic diseases or severe medically compromised. - Individuals with full dentures or crowns and bridges in occlusal contact with teeth indicated for the restorative treatment - Pregnant or lactating subjects, or intending to become pregnant during the course of the study - Poor oral hygiene. - Teeth with pulpal pain. - Teeth with periapical lesions. - Endodontically treated teeth - Teeth with mobility. - Non-functioning tooth with no opposing tooth. - Heavy occlusion or signs of severe attrition. - Severe periodontal affection

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ceram•X (Dentsply De Trey GmbH, Konstanz, Germany
The prepared cavities will be restored with Ceram•X (Dentsply De Trey GmbH, Konstanz, Germany) with incremental placement technique (maximum: 2-mm layer). Increments will be light curing for 20 seconds according to manufacturer's instructions.
Zenit Nano Ceramic Composite (PRESIDENT DENTAL, GmbH, Munich, Germany)
The prepared cavities will be restored with Zenit Nano Ceramic Composite (PRESIDENT DENTAL, GmbH, Munich, Germany) with incremental placement technique (maximum: 2-mm layer). Increments will be light curing for 40 seconds according to manufacturer's instructions.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Anatomic form Bravo: Restoration is under-contoured, without dentin or base exposure
Charlie: Restoration is under-contoured, without dentin or base exposure.restoration need replacement.
24 months
Secondary Color Match Alfa: Matches tooth. Bravo: Acceptable mismatch. Charlie: Unacceptable mismatch. 24 months
Secondary Marginal Discoloration Alfa: No discoloration. Bravo: minor marginal discoloration without staining toward pulp. Charlie: Deep discoloration with staining toward pulp. 24 months
Secondary Marginal Adaptation Alfa: Closely adapted, no visible crevice. Bravo: Visible crevice, explorer will penetrate. Charlie: Crevice in which dentin is exposed. 24 months
Secondary Secondary Caries Alfa: No active caries present. Bravo: Non-cavitated active caries is present in contact with the restoration. Charlie: Cavitated active caries is present in contact with the restoration. 24 months
Secondary Surface Texture Alfa: As smooth as the surrounding enamel. Bravo: Surface rougher than enamel, clinically acceptable. Charlie: Surface unacceptably rough. 24 months
Secondary Marginal Integrity Alfa: Restoration adapts closely to the tooth structure Bravo: A visible crevice. Charlie: The explorer penetrates into the crevice. 24 months
Secondary Postoperative sensitivity Alfa: No post-operative sensitivity. Bravo: Short term and tolerable post-operative sensitivity. Charlie: Intolerable post-operative sensitivity. 24 months
Secondary Amount of Restoration wear. Measuring unit: Microns (Quantitative) 24 months
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06107218 - Performance Of Class I Composite Restorations After Cavity Finishing By Air Abrasion Versus Diamond Stone N/A
Active, not recruiting NCT03184025 - Effect of Surface Sealant Application on Clinical Performance Occlusal Restorations N/A
Completed NCT05559333 - CLINICAL COMPARISON OF DIFFERENT GLASS IONOMER-BASED RESTORATIVES AND A BULK-FILL RESIN COMPOSITE IN CLASS I CAVITIES: A 48-MONTH RANDOMIZED SPLIT-MOUTH CONTROLLED TRIAL N/A