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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:
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.
Full description
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:
After rubber dam isolation and access cavity preparation, patients will be randomly assigned to one of four groups using a four-sided die.
Each group will consist of 22 patients and will undergo root canal shaping using an endomotor with one of the following techniques:
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:
The questionnaire will be held again with the VAS scores and percussion sensivity.
Final Root Canal Treatment:
Sample Handling:
Post-Treatment:
This standardized protocol ensures consistent data collection and optimal treatment outcomes for all participants.
Enrollment
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Primary purpose
Allocation
Interventional model
Masking
75 participants in 3 patient groups
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Central trial contact
Mustafa Mert Tulgar, Dmd; Emrah Karataşlıoğlu, PhD
Data sourced from clinicaltrials.gov
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