Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Age group 18-50 years
- Males and females
- Lower molars with symptomatic irreversible pulpitis without apical periodontitis
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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