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Evaluation of Different Root Canal Irrigation Techniques

M

Medipol University

Status

Completed

Conditions

Apical Periodontitis

Treatments

Procedure: Conventional Needle Irrigation
Device: EDDY Sonic Irrigation Activation
Device: VDW Ultra Ultrasonic Irrigation Activation

Study type

Interventional

Funder types

Other

Identifiers

NCT07106320
E-10840098-772.02-6497

Details and patient eligibility

About

This clinical study aims to evaluate the effect of different root canal irrigation techniques on postoperative pain levels and periapical healing in premolar and molar teeth diagnosed with apical periodontitis (Periapical Index (PAI) score 4-5). A total of 162 patients are randomly assigned to one of three groups: (1) sonic irrigation activation using EDDY, (2) ultrasonic irrigation activation using VDW Ultra, and (3) conventional syringe irrigation as the control. Postoperative pain will be recorded using the Visual Analog Scale (VAS) and Visual Analog Scale (VRS) at multiple time points up to one month. Periapical healing will be assessed using periapical imaging performed with the parallel technique one year after treatment. The study aims to determine whether enhanced irrigation techniques provide superior clinical outcomes compared to traditional methods.

Full description

Root canal treatment aims to eliminate microorganisms and their byproducts from the complex root canal system to allow periapical tissue healing. Due to the anatomical complexity of root canals-such as isthmuses, apical deltas, and lateral canals-mechanical preparation alone is often insufficient. Therefore, chemical irrigation plays a vital role in successful disinfection.

This randomized clinical trial investigates the influence of three different irrigation protocols on postoperative pain and periapical healing in permanent premolar and molar teeth with radiographically evident apical periodontitis (Periapical Index (PAI) score 4-5).

The study includes three experimental groups :

Group 1 (Sonic activation): Irrigation solution is activated using the EDDY sonic tip.

Group 2 (Ultrasonic activation): Irrigation is activated using VDW Ultra ultrasonic tips.

Group 3 (Control): Conventional needle irrigation is performed without activation.

All treatments will be performed under rubber dam isolation and local anesthesia, using a standardized instrumentation protocol with ProTaper Next rotary files. Between each file change, the root canal will be irrigated with 5 ml of 3% sodium hypochlorite (NaOCl). The final irrigation protocol will be applied according to the assigned group. All endodontic procedures will be completed in a single session.

Postoperative pain levels will be assessed using both the Visual Analog Scale (VAS) and Visual Analog Scale (VRS) scales at 6, 12, 18, 24, 48, and 72 hours, as well as on day 7 and at 1 month. Patients will be asked to record analgesic consumption (400 mg ibuprofen as needed) and will submit pain diaries.

One year after treatment, periapical healing will be evaluated using periapical radiography (parallel technique) by two blinded observers.

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Enrollment

162 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 60 years
  • Premolar and molar teeth with radiographically confirmed periapical lesions classified as Periapical Index (PAI) scores of 4 or 5 will be included in the analysis
  • Systemically healthy individuals
  • To be able to read and sign the informed consent form
  • Physical and mental fitness to undergo treatment
  • Willingness to attend all follow-up sessions

Exclusion criteria

  • Patients with systemic diseases classified as ASA III or higher
  • Presence of severe periodontal disease (probing depth >4 mm)
  • Use of analgesics within the last 12 hours or antibiotics within the past month before the treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

162 participants in 3 patient groups

Ultrasonic Irrigation Activation (VDW Ultra)
Experimental group
Description:
Irrigation will be activated using an ultrasonic device (VDW Ultra) with an IRRI S tip positioned 2 mm short of the working length. Final irrigation protocol: Each canal receives a total of 6 mL of 3% Sodium Hypochlorite (NaOCl), will be delivered in three separate 2 mL portions. Each portion will be activated for 20 seconds. Subsequently, 2 mL of 17% Ethylenediaminetetraacetic Acid (EDTA) will be introduced into per canal and similarly activated ultrasonically for 20seconds to facilitate smear layer removal. As a final rinse, 5 mL of sterile saline will be used to flush out any residual irrigants and prevent potential chemical interactions.
Treatment:
Device: VDW Ultra Ultrasonic Irrigation Activation
Sonic Irrigation Activation (EDDY)
Experimental group
Description:
Irrigation will be activated using a sonic device (EDDY tip, VDW) positioned 2 mm short of the working length. Final irrigation protocol: Each canal receives a total of 6 mL of 3% Sodium Hypochlorite (NaOCl), will be delivered in three separate 2 mL portions. Each portion will be activated for 20 seconds. Subsequently, 2 mL of 17% Ethylenediaminetetraacetic Acid (EDTA) will be introduced into per canal and similarly activated for 20 seconds to facilitate smear layer removal. As a final rinse, 5 mL of sterile saline will be used to flush out any residual irrigants and prevent potential chemical interactions.
Treatment:
Device: EDDY Sonic Irrigation Activation
Conventional Irrigation (Control)
Active Comparator group
Description:
Irrigation will be performed using a syringe and needle without activation. Final irrigation will be performed using conventional syringe and needle irrigation without any activation. Each canal will be irrigated with 6 mL of 3% Sodium Hypochlorite (NaOCl), followed by 2 mL of 17% Ethylenediaminetetraacetic Acid (EDTA) and 5 mL of sterile saline, using a side-vented needle.
Treatment:
Procedure: Conventional Needle Irrigation

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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