Post-operative Sensitivity in Resin Composites

Pakistan Institute of Medical Sciences

Status: Completed

Conditions: Caries,Dental; Sensitivity, Tooth

Treatments: Procedure: Group A(Nano-fortified Adhesive); Procedure: Group B(Adhesive without nanoparticles)

Study type: Interventional

Funder types: Other

Identifiers

NCT06242184

NAMIR

Details and patient eligibility

About

This triple-blind, randomized clinical trial was conducted at the department of Operative dentistry. A total of 60 participants were recruited and were randomly distributed into two groups A and B. After informed consent, restorative treatment was performed. In group A, adhesive with nanoparticles was used for composite restoration while in group B, adhesive without nanoparticles was utilized. Post-operative sensitivity was recorded using VAS score.

Full description

Triple-blind, randomized trial, parallel group with an allocation ratio 1:1. A total of 60 participants were recruited from the outpatient department and were randomly distributed into two groups (n=30). After informed consent, restorative treatment was accomplished using an etch and rinse adhesive strategy. In group A , titanium dioxide nano-fortified adhesive was used while in group B, adhesive without nanoparticles was utilized for composite restoration. Post-operative sensitivity was evaluated at follow-up period: one day, one week, two weeks and one month. Visual Analogue scale score was used to record the sensitivity status at follow-up intervals.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• participants with goof general health status
• Class I and II primary Carious lesion with a minimum cavity depth of 3 to 5 mm.
• Vital and Periodontally sound teeth

Exclusion criteria

• Patient with Temporomandibular dysfunction
• History of spontaneous pain
• Endodontically treated teeth
• Patient on analgesics within the past two weeks

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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60 participants in 2 patient groups

Group A (Nano-fortified Adhesive)

Experimental group

Description:

Titanium dioxide nanoparticles incorporated in dentin adhesive

Treatment:

Procedure: Group A(Nano-fortified Adhesive)

Group B (Adhesive without Nanoparticles)

Experimental group

Description:

Adhesive without nanoparticles

Treatment:

Procedure: Group B(Adhesive without nanoparticles)