Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
57 participants
INTERVENTIONAL
2024-02-12
2024-12-05
Brief Summary
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The null hypothesis is: "There is no difference in postoperative pain after root canal treatment between the irrigation activation systems in mandibular first molars and premolar teeth."
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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EDDY Group
The effect of the EDDY device, preferred for root canal irrigation activation, on postoperative pain formation
EDDY Group
The EDDY activation of the irrigation solutions used is performed to achieve root canal disinfection and enhance antibacterial effectiveness once the root canal preparation is completed.
PUI Group
The effect of the passive ultrasonic activation method, preferred for root canal irrigation activation, on postoperative pain formation
PUI Group
The passive ultrasonic activation of the irrigation solutions used is performed to achieve root canal disinfection and enhance antibacterial effectiveness once the root canal preparation is completed.
Control Group
Root canal treatment performed with conventional irrigation without the use of any activation method
No interventions assigned to this group
Interventions
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EDDY Group
The EDDY activation of the irrigation solutions used is performed to achieve root canal disinfection and enhance antibacterial effectiveness once the root canal preparation is completed.
PUI Group
The passive ultrasonic activation of the irrigation solutions used is performed to achieve root canal disinfection and enhance antibacterial effectiveness once the root canal preparation is completed.
Eligibility Criteria
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Inclusion Criteria
* Patients without pregnancy or breastfeeding status.
* Patients diagnosed with asymptomatic apical periodontitis confirmed through radiographic and clinical examination.
* Patients not having a regular intake of analgesic or anti-inflammatory drugs within the last 12 hours.
* Patients lacking a history of drug allergies.
* Teeth free from calcifications, resorptions, periodontal problems, incomplete root development, a history of endodontic treatment, traumatic occlusion, or severe coronal destruction.
* Teeth with a root canal curvature of 5° or less.
* Mandibular premolars and first molars.
Exclusion Criteria
* Teeth with an apical diameter larger than #20K file.
* Patients with a Periapical Index (PAI) score of 1 or 2.
* Teeth having extra canals.
* Teeth requiring a second local anesthesia during treatment.
* Teeth where a file fractured within the canal during preparation.
* Vital teeth.
* Patients reporting preoperative pain.
* Teeth showing clinical symptoms such as percussion or palpation sensitivity.
* Teeth with persistent purulent discharge.
18 Years
55 Years
ALL
Yes
Sponsors
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Ordu University
OTHER
Responsible Party
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Seca MUTLU
Research Assistant
Principal Investigators
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Seca MUTLU
Role: PRINCIPAL_INVESTIGATOR
Ordu University, Faculty of Dentistry, Department of Endodontics
Locations
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Ordu University
Ordu, Karadeniz, Turkey (Türkiye)
Countries
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Other Identifiers
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ODU-MUTLU-001
Identifier Type: -
Identifier Source: org_study_id