Actively Recruiting

Phase Not Applicable
Age: 19Years - 60Years
All Genders
Healthy Volunteers
ID06533215

Antimicrobial Efficacy of Nano-Based Intracanal Medications on Enterococcus Faecalis

Led by Tanta University · Updated on 2024-08-01

30

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the antimicrobial effects of new nano-based intracanal medications on reducing Enterococcus faecalis bacteria in patients with secondary endodontic infections. It focuses on cases where root canal treatments have failed due to persistent bacteria, particularly E. faecalis, which is common in infected root canals and known for its resistance and ability to survive harsh conditions. The study explores advanced treatment options using nanotechnology to improve disinfection outcomes in endodontic retreatment. The study compares three types of intracanal medications applied in retreatment cases: standard chlorohexidine gel, chlorohexidine loaded with silver nanoparticles gel, and triple antibiotic-loaded chitosan nanoparticles gel. These nano-formulated medications aim to enhance bacterial killing by leveraging the properties of nanoparticles. Participants receive one of these treatments applied inside the root canal to target the infection. Participants will undergo root canal retreatment on single-rooted premolar teeth with signs of infection. Samples from the root canal will be collected one week after medication application to measure the amount of Enterococcus faecalis bacteria. Researchers will also monitor post-operative pain during this period. The study uses bacterial cultures and clinical assessments to evaluate treatment effects and safety over a one-week follow-up, with total participation lasting about that time.

CONDITIONS

Brief Title

Antimicrobial Efficacy of Nano-Based ICM on E.F

Who Can Participate

Age: 19Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Single rooted, single canal premolar teeth
  • Teeth indicated for non-surgical root canal retreatment
  • Teeth with signs or symptoms of post-treatment disease such as recurrent acute or chronic periapical abscess
  • Teeth showing clinical signs of endodontic failure including sensitivity to percussion, pain, swelling, or fistula
  • Teeth with radiographic evidence of endodontic failure like persistent periapical lesions or widened periodontal ligament
  • Symptomatic or asymptomatic teeth with short root canal filling requiring prosthetic restoration
Not Eligible

You will not qualify if you...

  • Patients with any systemic diseases
  • Pregnant or lactating patients
  • Immunocompromised patients
  • Non-restorable tooth
  • Calcified root canal
  • Teeth with root fracture
  • Teeth with periodontal pocket deeper than 4mm
  • Teeth with procedural errors such as ledge, broken instrument, or perforation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 1 week

Participants receive intracanal medication with one of three types of gels to treat secondary endodontic infection cases and reduce Enterococcus faecalis bacteria.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 1 location

1

Faculty of Dentistry

Tanta, Egypt

Actively Recruiting

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Research Team

I

Ibrahim Ali, bachelor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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Frequently Asked Questions

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Published Research Related To This Trial

The antibacterial effect and the incidence of post-operative pain after the application of nano-based intracanal medications during endodontic retreatment: a randomized controlled clinical trial.

Mahmoud M Fahim, Shehab Eldin Mohamed Saber, Walid F Elkhatib...

https://pubmed.ncbi.nlm.nih.gov/34697657

Comparative evaluation of antimicrobial efficacy of triple antibiotic paste and calcium hydroxide using chitosan as carrier against Candida albicans and Enterococcus faecalis: An in vitro study.

Jaheer Shaik, Roopadevi Garlapati, Bolla Nagesh...

https://pubmed.ncbi.nlm.nih.gov/25125845