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Postoperative Dental PainNCT06760312

Effect of Different Apical Actions on Local Inflammatory Mediators and Pain

A study testing Root canal shaping with Continuous Rotation, Root canal shaping with Apical Reverse and Root canal shaping is conducted with Apical slow-down kinematic. in people with Postoperative Dental Pain and Pulp Disease, Dental, run by Izmir Katip Celebi University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 49 yearsHealthy volunteers can take part
What is being tested?
Root canal shaping with Continuous Rotation, Root canal shaping with Apical Reverse and Root canal shaping is conducted with Apical slow-down kinematic.
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
75 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Feb 2024to 1 Jul 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 49 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Mild, moderate pulpitis and pulpal expose patients in need of root canal -treatment to their mandibular premolars.
  • Healthy periodontal tissue with Periapical Index under 2.
  • Helathy adjacent teeth.

Who cannot join

  • Systemic diseases
  • Percussion pain
  • Patients who did not consent to a vital pulp therapy
  • Radiologically seen open apex, root resorption, calcification
  • Periodontal pocket beyond 4mm in length
  • Consumption of Antibiotics or Corticosteroids 1 month before the treatment
  • Consumption of antiinflammatory drugs 2 days before the treatment

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • İzmir Katip Çelebi Üniversitesi

    Izmir, Çiğli, 35649

Other trials in Turkey (Türkiye)

About this study

Official title: Effect of Different Apical Actions on Local Inflammatory Mediators and Pain During Root Canal Preparation: A Randomized Clinical Study

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?
Read more

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.

Read the detailed 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:

  • Patients will be asked about spontaneous pain and percussion pain related to the affected tooth prior to the session.
  • These pain levels will be recorded using the Visual Analog Scale (VAS).

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:
  1. Continuous Rotation
  2. Apical Reverse
  3. Apical Slow-Down

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:

  1. Working Length Determination: Establish the working length and create a glide path using a #10 K-file.
  2. Instrumentation Sequence: Enlarge the canals sequentially using rotary files of sizes 15.04, 20.04, 25.06, 30.06, and 35.06.
  3. Irrigation: Use 2 ml of 2.5% sodium hypochlorite (NaOCl) for irrigation after each file change.

Sample Collection (First Session):

  • After completing the first session:
  • Rinse the canals with distilled water.
  • Remove remaining liquid with #45 paper points.
  • Insert sterile #20.02 paper points into the canals and leave them for 30 seconds to collect periapical exudates.
  • Collect three samples per canal. Cut the apical 5 mm of the paper points and place them in 1.5 ml Eppendorf tubes for storage at -80°C.
  • The canals will then be rinsed again with 2.5% NaOCl. Patients will be dismissed without using intra-canal medication and instructed to return for the filling session after three days. Patients will be advised to take 800 mg ibuprofen if they experience pain. The medication use will be documented.

Second Session:

  • The questionnaire will be held again with the VAS scores and percussion sensivity.
  • After local anesthesia the intermediate restorative material is removed and root canal irrigation with distilled water.
  • Working length is confirmed again with a file. Collect three additional samples per canal using #20.02 paper points as in the first session.
  • Proceed to finalize the root canal treatment.

Final Root Canal Treatment:

  1. Perform the final irrigation using 2.5% sodium hypochlorite and 17% EDTA.
  2. Fit gutta-percha cones. 35.06 cone or fitting .02 tapered cones will be selected as the master cone according to the anatomy and fit.
  3. Fill the canals using a resin-based root canal sealer with lateral condensation utilizing #25 spreader and accessory #20.02 gutta-percha cones.
  4. After cutting the excess gutta-percha, clean the cavity and complete the treatment with composite resin restoration.

Sample Handling:

  • All collected samples will be stored in a -80°C freezer for biochemical analysis. The analysis will be based on ELISA tests which will investigate the Substance P, IL-1ß, TNF alpha and IL-6 on Day 0 and Day 3.

Post-Treatment:

  • The occlusion will be checked using articulation paper, and adjustments will be made if primary contact is present to ensure no traumatic occlusion.

This standardized protocol ensures consistent data collection and optimal treatment outcomes for all participants.

Being tested
Root canal shaping with Continuous Rotation, Root canal shaping with Apical Reverse, Root canal shaping is conducted with Apical slow-down kinematic.
Keywords
apical kinematics, apical action, apical reverse, apical slow-down, continuous rotation, Substance P, postoperative pain, Inflammation
Medical subject headings
Dental Pulp Diseases, Pain, Postoperative, Inflammation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Root canal shaping with Continuous RotationProcedure or surgery

    The root canal shaping is conducted with a continuous rotation kinematic.

  • Root canal shaping with Apical ReverseProcedure or surgery

    The root canal shaping is conducted with a apical reverse kinematic.

  • Root canal shaping is conducted with Apical slow-down kinematic.Procedure or surgery

    The root canal shaping is conducted with a apical slow-down kinematic.

Study groups in NCT06760312
Study groupRoleWhat they receive
Continuous RotationExperimentalThe apical root canal shaping mode of the apex locator integrated endodontic motor is "Continuous Rotation" which is the standard and mostly used option in endodontics. Works as a Control group also
Receives: Procedure: Root canal shaping with Continuous Rotation
Apical ReverseExperimentalThe apical root canal shaping mode of the apex locator integrated endodontic motor is "Reverse". The motor makes a reverse movement to prevent the file over the working length
Receives: Procedure: Root canal shaping with Apical Reverse
Apical Slow-downExperimentalThe apical root canal shaping mode of the apex locator integrated endodontic motor is "Apical Slow-down". The motor slows down the rotation to preserve the working length and apical constriction.
Receives: Procedure: Root canal shaping is conducted with Apical slow-down kinematic.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Substance P

    The local Substance P amount will be assesed with ELISA kits

    Measured: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.

Secondary outcomes (4)
  1. Visual Analog Scale

    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.

    Measured: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.

  2. Inflammatory Mediator: IL-1ß

    Local IL-1ß will be assessed with local collection from apical site.

    Measured: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.

  3. Inflammatory Mediator: IL-6

    Local IL-6 will be assessed with local collection from apical site.

    Measured: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.

  4. Inflammatory Mediator: TNF alpha

    Local TNF-alpha will be assessed with local collection from apical site.

    Measured: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jan 2025
  2. Study start1 Feb 2024
  3. Primary completion1 May 2025
  4. Study completion1 Jul 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
n=66 participants will be randomized into 3 different intervention groups.
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
75 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06760312
Sponsor's protocol ID
2023-KAE-0080
Status last verified
Jun 2025
First submitted
30 Dec 2024
Last updated
16 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: The patients' written consent also required that the data, which involves biological markers, be used only within the experiment and not shared with a third party.

Publications

  • Cohen, J (1988) Statistical power analysis for the behavioral sciences (2nd ed.). Hillsdale, NJ: Erlbaum

Questions about this trial

What is this clinical trial studying?

A study testing Root canal shaping with Continuous Rotation, Root canal shaping with Apical Reverse and Root canal shaping is conducted with Apical slow-down kinematic. in people with Postoperative Dental Pain and Pulp Disease, Dental, run by Izmir Katip Celebi University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Substance P (time frame: From Day 0 to Day 3. The last measurement will be taken just before the end of the interventional treatment.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06760312, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jul 2025; AzTrials last refreshed its copy on 6 Nov 2026.

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