İzmir Katip Çelebi Üniversitesi
Izmir, Çiğli, 35649, Turkey (Türkiye)
NCT Number: NCT06760312
The goal of this clinical trial is to determine patients' the inflammation and pain response to different apical actions used in rotary instrumentation during root canal shaping process. The main questions it aims to answer are:
1. How the different apical actions of endodontic motors influence the pain and inflammatory mediator release from the periapical region of related tooth? 2. Does the perceived pain differ among the used apical action methods after the root canal preparation? 3. Are the perceived pain and local pain mediator levels coherent?
Participants will:
Attend to the root canal treatment in the endodontics clinic. The treatment will be two visits.
Answer the Visual Analog Scale questionnaire on day 0 (first appt.) and Day 3 (second appt.) Keep a diary of their symptoms and the number of times they use an anti-inflammatory drug.
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Notify Me18 year–49 year
All sexes
Interventional
Not applicable
Izmir, Çiğli, 35649, Turkey (Türkiye)
Study Protocol
This study will include patients aged 18-49 years who present to the İzmir Katip Çelebi University, Department of Endodontics, requiring root canal treatment for vital, lesion-free mandibular first and second molars. Patients with systemic diseases will be excluded. The study will involve 66 patients. The sample size was calculated according to the effect size of 0,25 recommended by Cohen (1988).
Pre-Treatment Assessment:
Group Allocation:
Questionnaire:
Patients will be given a pen and will be asked to mark the current and percussion-provoked pain of the related tooth by a numbered linear Visual Analog Scale (VAS) before treatment on Day 0 and Day 3.
Root Canal Shaping:
Sample Collection (First Session):
Second Session:
Final Root Canal Treatment:
Sample Handling:
Post-Treatment:
This standardized protocol ensures consistent data collection and optimal treatment outcomes for all participants.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The root canal shaping is conducted with a continuous rotation kinematic.
The root canal shaping is conducted with a apical reverse kinematic.
The root canal shaping is conducted with a apical slow-down kinematic.
Time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.
The local Substance P amount will be assesed with ELISA kits
Time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.
Visual Analog Scale (VAS) questionnaire of perceived pain. A visual linear scale starting from 0 to 10. 0 represents no pain and 10 is the highest pain patient ever endured. Patient is asked to mark the pain in the scale.
Time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.
Local IL-1ß will be assessed with local collection from apical site.
Time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.
Local IL-6 will be assessed with local collection from apical site.
Time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.
Local TNF-alpha will be assessed with local collection from apical site.
Izmir Katip Celebi University
Other
Effect of Different Apical Actions on Local Inflammatory Mediators and Pain During Root Canal Preparation: A Randomized Clinical Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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