Evaluation of a New Bioactive Material Versus a Fluoride-Releasing Hybrid Restorative Material in Cervical Lesions

Dental Caries Clinical Trial

Official title:

One-Year Clinical Evaluation of a Fluoride, Calcium and Phosphate-Releasing New Bioactive Material Versus a Fluoride-Releasing Hybrid Restorative Material in Cervical Lesions: A Randomized Clinical Trial.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05149209
• Other study ID #: cons2021
• Status: Not yet recruiting
• Phase: N/A
• Start date: December 15, 2021
• Est. completion date: December 30, 2022

Study information

• Verified date: November 2021
• Source: Cairo University
• Contact: Nourhan K Mohamed, B.D.S
• Phone: 01003787886
• Email: nourhankhaled[@]dentistry.cu.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

• This study will be conducted to evaluate and compare the clinical performance of fluoride, calcium, and phosphate-releasing new bioactive material versus a fluoride-releasing hybrid restorative material in cervical lesions for one-year follow-up.

• The clinical evaluation will be done using modified USPHS criteria at baseline,3,6,9 and 12 months.

Description:

two groups of 30 patients will receive cervical restorations by using calcium and phosphate releasing hybrid restorative material (Activa™ Presto, Pulpdent®, USA), or a fluoride-releasing hybrid restorative material (Giomer, Shofu, Japan). Then these restorations will be evaluated at baseline, 3 months, 6 months, 9 months, and 12 months according to modified USPHS criteria in terms of marginal adaptation, Marginal discoloration, recurrent caries, retention, surface texture, and Post-operative sensitivity.

• Examination and selection of all patients will be done according to inclusion and exclusion criteria.

• A class v cavity will be prepared after local anesthesia has been given as required. Rubber dam isolation followed by the placement of restorative material according to the randomization sequence.

• For the intervention: selective etching to enamel and universal bond agent to all the cavity will be applied first, followed by filling of the cavity with fluoride, calcium, and phosphate-releasing new bioactive material (Activa™ Presto, Pulpdent®, USA) using a 19-gauge applicator tip on the syringe and light-curing for 20 seconds between each 2mm layer.

• For the control group: selective etching to enamel and universal bond agent to all the cavity will be applied first, followed by filling of the cavity with fluoride-releasing hybrid restorative material (Giomer, Shofu, Japan) and will be light polymerized using a light-emitting diode (LED) light-curing unit for 10 seconds between each 2mm layer.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: December 30, 2022
• Est. primary completion date: December 15, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• a)Inclusion Criteria of participants:

• Male or female gender.

• Only co-operative patients will be approved to participate in the trial.

• Medically free adult patients.

• The age range of the patients is 18-40 years. b)Inclusion Criteria of teeth:

• Small to moderate cervical lesion.

• Vital upper or lower teeth with no signs of irreversible pulpitis.

• Caries extension shouldn't exceed mesiodistal width and inciso(occluso)-gingival length not exceed incisal (occlusal) one third.

Exclusion Criteria:

• a)Exclusion criteria of participants:

• Allergic history concerning methacrylates

• Pregnancy

• Heavy smoking; xerostomia

• Lack of compliance

• Patients with disabilities.

• Patients having systemic diseases or severe medically compromised.

• Patients with severe bruxism, clenching, or temporomandibular joint disorders.

b)Exclusion criteria of the teeth:

• Deep defects (close to the pulp, less than 1 mm distance).

• Periapical pathology or signs of pulpal pathology.

• Possible prosthodontic restoration of teeth.

• Heavy occlusion and occlusal contacts or history of bruxism.

• Pulpitis, non-vital or endodontically treated teeth.

• Sever periodontal affection.

Related Conditions & MeSH terms

• Dental Caries

Intervention

Procedure:
• cervical restoration
A class v cavity will be prepared after local anesthesia has been given as required. Rubber dam isolation will be done. Selective enamel etching and a universal adhesive agent (Beautibond, Shofu, Japan) will be applied over all the cavity surfaces. Followed by, placement of restorative material according to the randomization sequence. Finally, restoration finishing and polishing will be done.

Locations

Country	Name	City	State
Egypt	Nourhan Khaled Mohamed Samir	Cairo	Maadi

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Marginal adaptation	The restoration will be clinically assessed by visual inspection and explorer. Restorations will be given a score using modified USPHS criteria: Alfa: Closely adapted, no visible crevice Bravo: Visible crevice, the explorer will penetrate Charlie: Crevice in which dentin is exposed	one year
Secondary	Marginal Discoloration	Clinical evaluation by visual inspection and mirror if needed using modified USPHS criteria. Restorations will be given the score: Alfa if No discoloration Bravo if Non penetrating marginal discoloration which can be polished away Charlie if Discoloration with penetration in pulpal direction.	one year
Secondary	Retention	Clinical evaluation by visual inspection and explorer. Restorations will be given a score according to modified USPHS criteria : Alfa if restoration is retained and there is no loss of restoration. Charlie if loss of restoration.	one year
Secondary	Secondary caries	Clinical evaluation by visual inspection and explorer. Restorations will be given a score according to modified USPHS criteria: Alfa if no recurrent caries is detected, charlie if recurrent caries is detected.; .	one year
Secondary	surface texture	Clinical evaluation by visual inspection and explorer. Restorations will be given a score according to modified USPHS criteria: Alfa if restoration is enamel-like surface Bravo if Surface rougher than enamel, clinically acceptable Charlie if Surface is unacceptably rough.	one year
Secondary	postoperative sensitivity	Verbal evaluation by asking the patient. Restorations will be given a score according to modified USPHS criteria: Alfa if not present Bravo if sensitive but diminishing in intensity Charlie if constant sensitivity not diminishing.	one year