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Recruiting NCT06640231

The Effect of XP-Endo Finisher Activation of Bioceramic Sealer on Postoperative Pain in Mandibular First Molar With Symptomatic Irreversible Pulpitis

No phase Interventional Symptomatic Irreversible Pulpitis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: sealer activation after cleaning and shaping with XP-Endo Finisher, negative control where canals are obturated directly without sealer activation.
Who it may be relevant to
Registry conditions: Symptomatic Irreversible Pulpitis. Basic parameters: 18 years — 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The aim of endodontic obturation is to make a complete sealing along the length of the root canal system to ensuring the peri radicular tissue healing and sustained health. Disadvantages of gutta-percha-based root filling materials is lack of adhesiveness to canal wall dentin. So, a sealer or cement has to be used with gutta-percha to achieve a fluid-tight seal and fill the space between the canal wall dentin and the obturating material. Drawbacks of resin-based sealer are difficult preparation technique of deep root canal cavity which also limit dentin bonding, difficult to be removed from the canal in retreatment cases and its shrinkage during setting. Bio-ceramic root canal sealers become popular in recent years because of their unique chemical and physical properties. These sealers are consisting of biocompatible materials that resemble the of tooth structure natural composition so bio-ceramic sealers are an ideal choice for root canal treatment. Bio-ceramic sealers are better than traditional sealers due to their multiple physical properties for example excellent sealing ability, dimensional stability, and low solubility. These properties ensure that the sealers achieve a tight seal, inhibiting bacterial leakage and decreasing the risk of reinfection. Diaroot Bioaggregate (DiaDent), a white nanoparticle-sized ceramic cement composed of calcium silicate, calcium hydroxide and hydroxyapatite and considered a modified version of MTA, with the advantage of being aluminium-free in composition, a fact that contributes to its greater biocompatibility with periradicular tissue.Root canal sealers activation may improve their penetration into dentinal tubules and improve sealability and antimicrobial effects. Recently, a non-tapered nickel-titanium rotary instrument (XP-endo Finisher; FKG, La Chaux-de-Fonds, Switzerland) has been designed to increase the efficiency in root canal wall cleaning specifically with limited impact on dentine throughout the literature, XP efficacy in decreasing microorganisms, dissolving organic tissue from artificial cavities in combination with NaOCl and penetrating into the isthmus has been analyzed. The aim of this study to evaluate the effect of XP-Endo Finisher activation of Bioceramic sealer on postoperative pain in mandibular first molar with symptomatic irreversible pulpitis. This study consists of 30 patients divided into 2 group each group having 15 patients. Intervention: Bioceramic sealer activation with XP Endo Finisher. Control group: Bioceramic sealer without activation.

Interventions

  • Other sealer activation after cleaning and shaping with XP-Endo Finisher
    activation of sealer before the obturation of root canals
  • Other negative control where canals are obturated directly without sealer activation
    sealer after cleaning and shaping before the obturation without using activation method

Primary outcome measures

  • Post-operative pain after sealer activation with XP-Endo Finisher in comparison to without sealer activation [Time frame: Immediately after obturation, 6-, 12-, 24- and 48-hours post-operative.]
Secondary outcome measures (1)
  • Number of analgesic tablets taken after endodontic treatment with sealer activation in comparison to without sealer activation [Time frame: Up to 48 hours postoperatively.]

Eligibility criteria

Inclusion criteria

  • Age ranges from 18 to 40 years old.
  • No sex predilection.
  • Patients seeking root canal treatment.
  • Systematically healthy patient (ASA I, II).
  • Patient who can understand numerical rate scale and sign an informed consent.
  • Mandibular first molar teeth with:
  • Preoperative sharp (moderate or severe) pain.
  • Vital response of pulp tissue to cold pulp tester (ethyl chloride spray).
  • Normal periapical radiographic appearance.

Exclusion criteria

  • Patients with American association of anesthesiologists (ASA) classification other than ASA T\& II.
  • Patients who have already ingested preoperative medication, such as analgesics, non-steroidal or steroidal anti-inflammatory drugs, within 12 hours of the start of treatment.
  • Patients with NSAIDs allergy.
  • Patients having two or more adjacent teeth needing root canal therapy.
  • Pregnant patients.
  • Patients with bleeding disorder.
  • Patients with long term corticosteroid use
  • Teeth having;
  • Necrotic pulp.
  • History or presence of swelling or fistulous tract.
  • Acute / chronic periapical abscess.
  • Mobility more than grade 1.
  • Pocket depth more than 5mm.
  • No possible restorability.
  • Previous root canal treatment.
  • Periapical radiolucency.
  • External or internal resorption.
  • Vertical root fracture.
  • TMJ problems, bruxism, clenching or traumatic occlusion.
  • Inability to understand and perform the given instructions.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Future University in Egypt — Cairo

Identifiers

NCT: NCT06640231 · FUE.REC(21)/7-2024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗