Chronic Apical PeriodontitisPhase 4NCT06860191
Effect of Different Sealers and Activation Methods on Pain
A Phase 4 study testing Root Canal Sealants in people with Chronic Apical Periodontitis, run by TC Erciyes University.
Trial summary
In this study, the effects of different irrigation agitation methods and different root canal filling sealers on postoperative pain after root canal treatment will be evaluated. Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Chronic Apical Periodontitis
- What is being tested?
- Root Canal Sealants
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- No sites listed yet
- Study dates
- 1 Mar 2025to 1 May 2025
- Phase
- Phase 4
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 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Patients aged 18-60 years who are classified as medically healthy (ASA I or II),
- Teeth that do not need periodontal and prosthetic treatment, with a periapical index score between 2 and 4,
- Teeth with single root and canal diagnosed with asymptomatic apical periodontitis,
- Teeth that respond negatively to electric pulp test (Parkell) or cold test (Endo Ice; Coltene, Altstätten, İsviçre), without pain during percussion and palpation.
Who cannot join
- Teeth with PAI scores lower than 2
- Patients who had taken analgesics or anti-inflammatory drugs in the last 4 hours
- Diabetic, immunocompromised, pregnant or history of antibiotic use in the last month or patients receiving antibiotic prophylaxis
- Teeth with root resorption, immature, severe crown damage, calcified canals, and previous root canal fillings
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Evaluation of the Effects of Different Root Canal Sealer and Irrigation Agitation Methods on Postoperative Pain in the Treatment of Teeth with Chronic Apical Periodontitis - Prospective Randomized Clinical Trial
In this study, the effects of different irrigation agitation methods and different root canal filling sealers on postoperative pain after root canal treatment will be evaluated.
Read the detailed description
Root canal obturation is fundamental to successful root canal treatment. The primary objectives of root filling are to inhibit the growth of residual microorganisms following chemomechanical disinfection, prevent apical and coronal microleakage, and facilitate periapical tissue healing through appropriate materials and techniques. However, the intricate anatomy of the root canal system, including dentinal tubules, irregularities, and accessory canals, presents significant challenges to attaining an ideal root filling. Typically, this procedure uses a combination of core materials, such as gutta-percha, and root canal sealer. Sealers fill the spaces between the core material and the canal walls, ensuring a comprehensive three-dimensional filling that isolates any remaining bacteria and mitigates the risk of recontamination, reducing the likelihood of apical periodontitis.
In addition to their sealing function, root canal sealers exhibit antimicrobial properties and biocompatibility, which vary depending on their chemical composition. They are categorized based on their components into bioceramic-based, calcium hydroxide-containing, glass-ionomer-based, resin-based, silicone-based, and zinc-oxide eugenol sealers. Among these, epoxy-resin-based sealers, such as AH Plus, are widely recognized for their favorable physical properties, including low solubility and dimensional stability, often serving as benchmark materials for the evaluation of alternative sealers. Although AH Plus, an epoxy-resin-based sealer, is widely used in root canal treatment, it can lead to inflammation and pain if it comes into contact with periodontal tissues. In contrast, today bioceramic-based root canal sealers are gaining popularity due to their advantageous bioactive properties. These include antibacterial activity facilitated by an alkaline pH, promoting apical healing through hydroxyapatite formation, dentine structure mineralization, and effective sealing capabilities. Due to their hydrophilic nature, fine particle size, and ability to promote mineralized tissue formation, calcium silicate sealers provide excellent adaptation to canal walls, ensuring an effective seal and contributing to the overall success of the treatment. NeoSealer Flo is a bioactive ceramic paste that is premixed and contains a fine grade of inorganic powder made from tricalcium and dicalcium silicate. It is radiopaque, free from resin, and non-discoloring, and was formulated to harden when moisture from dentinal tubules is present. It possesses antimicrobial properties in vitro due to its high initial pH.
Nickel-titanium systems are recognized for their safety and efficiency. However, no preparation system can eliminate gutta-percha and sealers from canal walls. To address this limitation, various techniques to more effectively remove residual materials from root canals. These systems aim to enhance canal disinfection, improve solution penetration into the apical delta and lateral canals, and mitigate resistant bacterial strains that complicate dentinal tubular disinfection. Manual dynamic agitation (MDA), passive ultrasonic agitation (PUA), and sonic agitation are among the most commonly utilized activation techniques. During root canal preparation, using gutta-percha matching the diameter of the final file creates a dynamic irrigation effect through hydrodynamic activity generated by its oscillation in the irrigation solution. The MDA technique enhances debridement by improving the interaction between the irrigant and canal walls. PUA, introduced as an activation technique in the final stage of root canal treatment, offers multiple advantages. Systems like Ultra X enhance debris removal, microorganism elimination, and smear layer cleaning through high-speed flow, allowing the irrigant to reach accessory canals effectively without causing dentin damage. PUA achieves this by transmitting acoustic energy via ultrasonic waves through an oscillating file or wire, inducing two key actions: acoustic streaming, which generates hydrodynamic forces, and cavitation, where vapor-filled bubbles form within the fluid. Combining PUA with irrigants such as NaOCl, EDTA, and CHX has proven highly effective against E. faecalis.
There is insufficient data on the efficacy of adding MDA or PUA to the final irrigation protocol on postoperative pain after the single-visit endodontic treatment in cases with chronic apical periodontitis. Furthermore, there is a study in the literature regarding the potential effects of calcium-silicate-based NeoSealer Flo on postoperative pain. The purpose of this study is to evaluate the effect of different irrigation agitation techniques used in conjunction with resin-based (Ah Plus) and calcium silicate-based (NeoSealer Flo) sealers on postoperative pain in the treatment of chronic apical periodontitis.
The first null hypothesis of this study is that there is no statistically significant difference in treatment success, pain intensity, or frequency of occurrence following single-visit root canal treatment using AH Plus and NeoSealer Flo. The second null hypothesis is that there will be no statistically significant difference in postoperative pain intensity between the irrigation agitation techniques (MDA and PUA).
- Conditions
- Chronic Apical Periodontitis
- Being tested
- Root Canal Sealants
- Keywords
- Caries, apical periodontitis, irrigation agitation, root canal sealer
- Medical subject headings
- Periapical Periodontitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Root Canal SealantsDrug
In this study, different irrigation agitation methods and different root canal sealers will be compared.
| Study group | Role | What they receive |
|---|---|---|
| Ah plus+MDA | Experimental | Ah plus will be used as the root canal sealer and manual dynamic activation will be used for irrigation agitation. Receives: Drug: Root Canal Sealants |
| Ah plus+PUA | Experimental | Ah plus will be used as the root canal sealer and pasive ultrasonic agitation will be used for irrigation agitation. Receives: Drug: Root Canal Sealants |
| Neosealer Flo+MDA | Experimental | Neosealer Flo will be used as the root canal sealer and manual dynamic activation will be used for irrigation agitation. Receives: Drug: Root Canal Sealants |
| Neosealer Flo+PUA | Experimental | Neosealer Flo will be used as the root canal sealer and pasive ultrasonic agitation will be used for irrigation agitation. Receives: Drug: Root Canal Sealants |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pain symptoms of the patients will be evaluated with prepared questionnaires, and periapical lesion healing will be evaluated with periapical radiographs. A visual analog scale will be used to measure the degree of pain.
Performing clinical and radiographic follow-up and evaluation of the patient.A visual analog scale will be used to measure the degree of pain.
Measured: 1-4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Mar 2025
- Study start1 Mar 2025 (estimated)
- Primary completion1 Mar 2025 (estimated)
- Study completion1 May 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Apical PeriodontitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- TC Erciyes University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ipek Eraslan Akyuz, TC Erciyes University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06860191
- Sponsor's protocol ID
- 2025/1
- Status last verified
- Feb 2025
- First submitted
- 1 Feb 2025
- Last updated
- 5 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: It was decided that it was appropriate to keep participant information confidential until the study was completed.