NCT06242184

Post-operative Sensitivity in Resin Composites

Post-operative Sensitivity in Composites Using Bacillus Subtilis Procured Novel Nano-fortified Adhesive: a Triple-blind Study

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 60 (actual)
• Sponsor: Pakistan Institute of Medical Sciences · Other Government
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

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.

Detailed 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.

Conditions

• Caries,Dental
• Sensitivity, Tooth

Interventions

Type	Name	Description
PROCEDURE	Group A(Nano-fortified Adhesive)	Nano-fortified dentin adhesive
PROCEDURE	Group B(Adhesive without nanoparticles)	Conventional adhesives without nanoparticles

Timeline

• Start date: 2023-05-15
• Primary completion: 2023-11-25
• Completion: 2023-11-25
• First posted: 2024-02-05
• Last updated: 2024-02-06

Locations

1 site across 1 country: Pakistan