MedTrace Logo

Post-operative Sensitivity in Resin Composites

NCT06242184 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-02-06

No results posted yet for this study

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.

Conditions

  • Caries,Dental
  • Sensitivity, Tooth

Interventions

PROCEDURE

Group A(Nano-fortified Adhesive)

Nano-fortified dentin adhesive

PROCEDURE

Group B(Adhesive without nanoparticles)

Conventional adhesives without nanoparticles

Sponsors & Collaborators

  • Pakistan Institute of Medical Sciences

    lead OTHER_GOV

Principal Investigators

  • Nehal Amir, BDS · Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-15
Primary Completion
2023-11-25
Completion
2023-11-25

Countries

  • Pakistan

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06242184 on ClinicalTrials.gov