Post-operative Sensitivity in Resin Composites

Status Completed

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06242184
Study type	Interventional
Source	Pakistan Institute of Medical Sciences
Contact
Status	Completed
Phase	N/A
Start date	May 15, 2023
Completion date	November 25, 2023

View Details

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT05792800` - Dental Practitioners KAP Regarding Caries Preventive Measures in Cairo and Riyadah
Not yet recruiting	`NCT05792215` - KAP of Dental Practitioners Regarding CRA
Withdrawn	`NCT04104789` - Kovanaze Vs. Articaine in Achieving Pulpal Anesthesia of Maxillary Teeth - General	Phase 2
Active, not recruiting	`NCT06211582` - Clinical Performances of 3-different Tooth-colored Restorative Materials in Class-II Cavities	N/A
Active, not recruiting	`NCT04342858` - Prospective Randomized Controlled Trial for Prevention of Demineralization During Fixed Orthodontic Treatment	Phase 2
Recruiting	`NCT05362461` - Diagnostic Ability of Near Infrared Transillumination Detecting Interproximal Caries as Compared to Conventional Bitewing Radiographs
Not yet recruiting	`NCT04422860` - Remineralization Efficacy of Gum Arabic Varnish.	Phase 2/Phase 3
Not yet recruiting	`NCT06063239` - Probiotics in Special Needs Patients at High Risk for Tooth Decay: a Randomized Controlled Trial.	N/A
Completed	`NCT04286256` - Using Motivational Interviewing To Reduce Parental Risk-Related Behaviors For Early Childhood Caries	N/A
Completed	`NCT06182267` - Maximal Use Study to Determine the Pharmacokinetics of L-arginine After Exaggerated Oral Use of COL101	Phase 1
Not yet recruiting	`NCT03671200` - Correlation Between Caries Experience in Primary Molars and First Permanent Molars
Not yet recruiting	`NCT06365281` - Caries Prevalence, Experience and Risk Related Factors Among Early Middle-aged Patients Attending Cairo University
Completed	`NCT04003493` - LifE Style, Nutrition and Oral Health in Care Givers (LENTO)	N/A
Enrolling by invitation	`NCT04251858` - Evaluation of Oral Condition and the Effect of Dental Treatment on Physical Parameters of Athletes	N/A
Terminated	`NCT01796106` - Clinical Trial Proximal Caries Infiltration and Detection	N/A
Not yet recruiting	`NCT05943782` - Evaluation of CAD/CAM Onlays Fabricated by Subtractive Versus Additive Digital Manufacturing Techniques.	N/A
Recruiting	`NCT06114030` - Clinical and Radiographical Evaluation of CAD-CAM Crowns With and Without Deep Margin Elevation	N/A
Recruiting	`NCT05756413` - Birth to Three - Cavity Free	N/A
Not yet recruiting	`NCT04303767` - The Effect of Casein Phosphopeptide Amorphous Calcium Phosphate on Affected Dentine	Phase 2
Completed	`NCT05231330` - Clinical Evaluation of Silver Nanoparticles in Comparison to Silver Diamine Fluoride in Management of Deep Carious Lesions	N/A