Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID06573710

Correlation Between Postoperative Pain and Apical Extrusion of Different Irrigation Activation Techniques Randomized Controlled Trial - an In Vitro Study

Led by Ain Shams University · Updated on 2024-08-27

32

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of different irrigant activation techniques on postoperative pain in patients with vital teeth suffering from symptomatic irreversible pulpitis. This trial also assesses the amount of debris extrusion at the root tip, which may relate to pain levels after treatment. The study includes several methods for activating root canal irrigants to compare their impact on patient discomfort and debris removal. Participants will receive one of four treatments: laser activation using a diode laser, sonic activation with a polyamide EDDY tip, ultrasonic activation with an ED60 tip, or passive irrigation using a side-vented endodontic needle. Each technique involves specific timing and movement protocols for activating the irrigant within the root canal, followed by irrigation with a 17% EDTA solution. The trial combines a randomized controlled clinical study with an in vitro analysis of debris extrusion. During the study, participants will report their pain levels before and after treatment at multiple time points: 8, 24, and 48 hours, and one week post-procedure. Researchers will also monitor the frequency of pain medication use during this period. The trial is designed as a single-blind, randomized controlled trial sponsored by Ain Shams University, with participants aged 18 to 50 years. Overall, the study aims to correlate postoperative pain with the amount of debris pushed out during root canal irrigation.

CONDITIONS

Brief Title

Correlation Between Postoperative Pain and Apical Extrusion of Different Irrigation Activation Techniques

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age group 18-50 years
  • Males and females
  • Lower molars with symptomatic irreversible pulpitis without apical periodontitis
Not Eligible

You will not qualify if you...

  • Patients with uncontrolled health conditions
  • Immunocompromised patients
  • Teeth with periodontal diseases
  • Teeth with calcified canals
  • Pregnant patients

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.

Treatment

Duration - Single day procedure with follow-up for 1 week

Participants receive different irrigation activation techniques during dental procedures to evaluate postoperative pain and analgesic use.

1 treatment visit and 4 follow-up visits at 8, 24, 48 hours and 1 week

Trial Site Locations

Total: 1 location

1

Ain Shams University

Cairo, Egypt

Actively Recruiting

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Research Team

O

Omnia Hani Mohamed Tawfik

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

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