Modulation of Periapical Inflammation Following Nano-sized Intracanal Medication. A Randomized Controlled Clinical Trial (Nano-Chitosan)

May 3, 2026 updated by: Sabah Morad Sobhy, Al-Azhar University

Modulation of Periapical Inflammation Following Nano-Calcium Hydroxide and Nano-Chitosan Intracanal Medications in Endodontic Retreatment Cases: A Randomized Controlled Clinical Trial

The main cause of endodontic disorders is microbial infection. From the infected pulp tissue, microorganisms can penetrate into the deeper layers of root dentine and propagate a periapical tissue through the apical foramen and lateral canals causing apical periodontitis. Apical periodontitis is an inflammatory condition affecting the periapical area of teeth with a global prevalence of 52% among individuals and 5% at tooth level. At the periapical region, microbes and their products encounter the host immune defense. Innate immune cells combat bacteria through phagocytosis and release anti-microbial substances, while adaptive immune cells initiate both cell-mediated and humoral immune responses. This immune activation also stimulates osteoclasts, leading to bone resorption and creating space for the inflammatory cells' infiltration . During periapical inflammation, immune cells migrate to the periapical area, where they release pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), along with anti-inflammatory cytokines like interleukin-10 (IL-10). These cytokines play crucial roles in modulating inflammation and tissue repair.

MicroRNAs (miRNAs) are evolutionarily conserved small (18-22 nucleotides) single-stranded, noncoding RNAs. It has been well acknowledged that miRNAs influence gene expression at the posttranscriptional level by targeting mRNA 3'-untranslated regions (3'-UTRs). Accumulating evidence has suggested that miRNA expression is related to the clinical and biological features of diverse diseases, and they can be potential biomarkers for diagnosis, treatment, and prognosis. miRNAs have revealed their critical roles in regulating various cellular functions, including proliferation, apoptosis, differentiation, metabolism, and tumorigenesis, by targeting specific mRNAs.

MiR-146a regulates innate immunity, inflammatory responses, and the antiviral pathway. Changes in miR-146a expression have been noted in many human diseases, including autoimmune disorders and cancers. In addition, miR-146a is an important biomarker of disease diagnosis, prevention, and treatment. It is a negative regulator of inflammatory responses by suppressing target gene expression. However, limited data is available regarding the functional role of miR-146a in modulating the inflammatory response of periapical tissues following root canal disinfection in endodontic retreatment cases.

Eliminating microorganisms is the primary objective of root canal therapy in order to create an environment as free of bacteria as possible. However, not all root canal treatments are completely successful, and in some cases, the infection persists leading to development of secondary apical periodontitis in previously treated teeth.

Disinfecting the root canal during retreatment is significantly more challenging due to the presence of persistent microorganisms that have settled in the root canal system. These microbes are often resistant to standard irrigations and antimicrobial agents leading to the formation of periradicular lesions. Such bacteria can survive for extended periods around the previously filled root canals. Sodium hypochlorite (NaOCl) is the most widely used irrigant in root canal therapy due to its strong antibacterial effect and its ability to dissolve organic substances. Effective canal cleaning is difficult to achieve without the use of NaOCl at a sufficiently high concentration. However, NaOCl has several drawbacks, including its cytotoxicity which can lead to tissue damage and patient symptoms. Additionally, its strong oxidizing nature negatively affects the mechanical properties of dentin such as microhardness and elastic modulus. NaOCl should be used with caution in endodontic procedures to prevent hypochlorite accidents.

Calcium hydroxide (Ca (OH)2) is the most widely utilized intracanal medication. It has the potential to dissolve tissue, acts as a physical barrier and generates hydroxyl ions, creating an extremely alkaline environment. It has been shown to be quite effective in the treatment of teeth with persistent periapical lesions. To provide optimal endodontic treatment, the root canal system should be thoroughly cleaned of soft-tissue debris, smear layer, and bacteria. Nanoparticles (NPs) have unique characteristics such as smaller sizes, increased surface area to volume ratio, and higher chemical reactivity and charge density leading to greater interaction with the environment and negatively charged bacterial cells, compared to their bulk counterparts. These advantages can be used to design highly anti-microbial agents with maximal therapeutic efficacy and minimal side effects.

Study Overview

Detailed Description

Sixty-three patients will be divided randomly into three groups (21 patients in each group) using simple randomization procedure using random number generator. https://www.random.org/ based on intracanal medicament used. Sequentially numbered opaque sealed envelopes prepared in advance by an independent researcher will be used to prevent prediction of group assignment.

After application of local anesthesia (4% articaine with 1:100,000 epinephrine) and rubber dam isolation, the crown surfaces will be swabbed using 3% hydrogen peroxide, 5.25% sodium hypochlorite and 5% sodium thiosulphate before and after endodontic access. Gutta percha removal will be performed, the working length will be determined using an electronic apex locator (EAL) and will be confirmed using periapical radiograph, then the pre-instrumentation periapical samples (S1) will be gathered with a sterile #15 paper point. Root canal preparation will be performed using ProTaper Next nickel-titanium rotary system (Dentsply, Maillfer, Switzerland) driven by EndoEst motor mini (Geosoft Dent., Russia) endomotor till size X5 (50.05) file in continuous rotation at 300 rpm and 2 Ncm. After each file use, the root canal will be irrigated with 5ml of freshly prepared 2.5% sodium hypochlorite (NaOCl) solution (Alex. Deteregents and Chemical Co., Egypt) for 1 minute using a 31-gauge Navi-Tip flexible irrigating needle (Navi-Tip, Ultradent product, South Jourdan, UT). 5 ml of 17% EDTA (Colgate Oral Care Company, Waverly, Australia) for 1 min will be used for smear layer removal following saline separation. 5 ml of saline solution will be used for final irrigation of the root canal to neutralize all the previously used irrigants and post-instrumentation samples (S2) will be taken using #40 paper points.

Subsequently, three groups will be formed according to the predetermined group numbers based on intracanal medicament used. Group I: Nanochitosan paste (Nanogate company, Cairo, Egypt), Group II: Nano-calcium hydroxide paste (Nanogate company, Cairo, Egypt), Group III: Calcium hydroxide paste (MetaBiomed, Chungcheongbuk-do, Korea) in its regular form. Intracanal medicament will be placed in the canal, 1 mm shorter than the working length using the applicator tip and left for 1 week. The access cavity will be temporarily sealed with light cure glass ionomer resin cement. After 1 week, the temporary filling will be removed following local anaesthesia and isolation, the root canal will be irrigated with 20 ml saline and gently filed using H file corresponding to the master apical file size. The last sample (S3) will be collected using #40 paper points. During sampling, each paper point will be introduced into the canal 2 mm beyond the working length for 1 min. The root canals will be flushed with phosphate buffered saline (PBS) solution when blood or purulent discharge is detected or if the canal is dry and sampling will be repeated. The samples will be transferred in a sterile tube and stored at -80°C until processing(24).

The operator will be informed of the assigned group only immediately prior to medicament application. It will follow triple-blind design, in which the patient, outcome assessor and statistician are blinded to group allocation.

Finally, the root canal system will be obturated using ADSEAL resin-based sealer (Meta Biomed Co, Cheongju, Korea) and gutta-percha (Protaper next; Dentsply Maillefer, Switzerland) with cold lateral condensation method after being completely dried using paper points of comparable size to the master cone. A final coronal restoration with direct composite filling (Filtek Bulk Fill,3M ESPE, USA) will be performed in the same visit.

Potential harms include:

  • Mild postoperative pain or discomfort
  • Irritant reaction to irrigants or medicaments
  • Temporary inflammation flare-up

Risk minimizing measures:

  • Strict rubber dam isolation
  • Standardized irrigation protocols
  • Analgesic and antibiotic prescription if needed

An interim analysis will be conducted after 50% recruitment. The trial will be stopped early if:

• Severe adverse events exceed 10% in any group Statistically significant superiority or harm is detected

A data safety monitoring committee composed of an independent endodontist, pathologist, will oversee safety.

Adverse events will be documented at each visit and reported to the ethics committee within 48 hours for serious events.

Participants will be withdrawn in case of development of acute infection requiring antibiotics, severe pain requiring analgesics, failure to attend follow up appointment and protocol violation affecting outcome validity.

Study Type

Interventional

Enrollment (Estimated)

63

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Nasr City
      • Cairo, Nasr City, Egypt, 11765
        • Recruiting
        • Al Azhar University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Patients have single rooted teeth with root canal form type I. Have previous endodontic therapy with failure. Have periapical radiolucency (PAI score of 3 or 4). Asymptomatic patients who had no pain or swelling, had a negative response to palpation and percussion.

Exclusion Criteria:

Patients who had received antibiotic therapy within the past 3 months. Pregnancy and lactation. Systemic disease. Physical or mental disability. Non-restorable teeth. Any signs of resorption, immature roots, fracture, sinus tract and dental anomaly

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group I: Nanochitosan paste
Intracanal medicament will be placed in the canal, 1 mm shorter than the working length using the applicator tip and left for 1 week.
Nanochitosan paste (Nanogate company, Cairo, Egypt)
Experimental: Group II: Nano-calcium hydroxide paste
Intracanal medicament will be placed in the canal, 1 mm shorter than the working length using the applicator tip and left for 1 week.
Nano-calcium hydroxide paste (Nanogate company, Cairo, Egypt),
Experimental: Group III: Calcium hydroxide paste
Intracanal medicament will be placed in the canal, 1 mm shorter than the working length using the applicator tip and left for 1 week.
Calcium hydroxide paste (MetaBiomed, Chungcheongbuk-do, Korea)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
IL-10 and TNF-α levels
Time Frame: 1 week
IL-10 and TNF-α levels will be quantified using ELISA kit from periapical fluid samples according to manufacturer instructions and regulatory miR-146a will be quantified using Real-time PCR
1 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Periapical cytological smear
Time Frame: 1 week
Periapical cytological smear will be obtained using paper points. The paper points will be rolled onto a clean glass slide, stained and examined microscopically for the presence of inflammatory cells.
1 week
Postoperative pain assessment
Time Frame: 1 week

Pain intensity will be assessed using the Visual Analog Scale (VAS) on a 10-point scale (0 = no pain, 10 = worst pain imaginable) at the following timepoints:

  • Pre-treatment (baseline).
  • 6 hours post-treatment.
  • 12 hours post-treatment.
  • 1st day post-treatment.
  • 2nd day post-treatment.
  • 3rd day post-treatment.
  • 7th day post-treatment.
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Cicek E, Koçak MM, Kocak S, Saglam BC, Turker SA. Postoperative pain intensity after using different instrumentation techniques: a randomized clinical study. J Appl Oral Sci. 2017; 25: 20-6.
  • Zand V, Mokhtari H, Hasani A, Jabbari G. Comparison of the penetration depth of conventional and nano-particle calcium hydroxide into dentinal tubules. Iran Endod J 2017;12: 366-70.
  • Waltimo T, Trope M, Haapasalo M, Orstavik D. Clinical efficacy of treatment procedures in endodontic infection control and one-year follow-up of periapical healing. J Endod 2005; 31:863-6.
  • Shrestha A, Kishen A. Antibacterial nanoparticles in endodontics: A systemic review. J Endod 2016; 42:1417-26.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2026

Primary Completion (Estimated)

January 15, 2027

Study Completion (Estimated)

January 30, 2027

Study Registration Dates

First Submitted

March 15, 2026

First Submitted That Met QC Criteria

May 3, 2026

First Posted (Actual)

May 6, 2026

Study Record Updates

Last Update Posted (Actual)

May 6, 2026

Last Update Submitted That Met QC Criteria

May 3, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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