Influence of Apical Patency Concept Upon Postoperative Pain After Root Canal Treatment

Overview

The aim of this clinical study is to evaluate the influence of apical patency concept implementation upon postoperative pain following root canal treatment in a single visit approach in molars with pulpal disease.

Full Title of Study: “Influence of Apical Patency Concept Upon Postoperative Pain After Root Canal Treatment in Molars With Pulpal Disease. A Randomized Controlled Clinical Trial.”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Prevention
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: December 30, 2021

Detailed Description

All patients will be treated in a single session approach regardless of the group. All molars will be anesthetized either through infiltration in case of maxillary molars or inferior alveolar nerve block in case of mandibular molars using Octocaine 2% with epinephrine 1: 100,000 (Lidocaine HCl, Novocol Pharmaceutical, Ontario, Canada.). Rubber dam will be applied; and access will be opened using Endo access bur. Canals will be scouted using manual patency file in a watch winding maneuver and then coronal flaring will be performed using Gates Glidden drill #3 in a brushing motion away from dangerous zone. Root canals will be copiously irrigated using 10 ml 2.5% sodium hypochlorite NaOCl (Clorox; Egyptian Company for household bleach, Egypt) delivered using 28 Gauge safety Steri Irrigation Tip (DiaDent Group International, Burnaby, BC, Canada) inserted 3 mm below cementoenamel junction. Working length will be determined using electronic apex locator Root ZX II (J. Morita Mfg. Corp, Kyoto, Japan) and confirmed radiographically using parallel technique with receptor holding device. Canals will be irrigated again with 10ml 1.5% NaOCl, which will be delivered 2mm coronal to apical canal terminus. Irrigation will be hydro-dynamically agitated with EndoActivator device (Dentsply Maillefer, Baillagues, Switzerland) using yellow tips #20/06 inserted 2mm short of working length for 60 seconds. Root canals will be shaped using ProTaper next rotary Ni-Ti files (Dentsply Maillefer, Baillagues, Switzerland). In Gp A, apical patency will be maintained till obturation using electronic apex locator confirmed radiographically while in Gp B apical patency will not be maintained. Finally, Root canals will be obturated using cold lateral compaction technique. The molars will be permanently restored using composite resin restoration and will be scheduled for extra coronal restoration.

Interventions

  • Procedure: apical patency
    • In Gp A, apical patency will be maintained till obturation using electronic apex locator confirmed radiographically. Finally, Root canals will be obturated using cold lateral compaction technique. The molars will be permanently restored using composite resin restoration and will be scheduled for extra coronal restoration.
  • Procedure: Non-apical surgery
    • in Gp B apical patency will not be maintained. Finally, Root canals will be obturated using cold lateral compaction technique. The molars will be permanently restored using composite resin restoration and will be scheduled for extra coronal restoration

Arms, Groups and Cohorts

  • Experimental: Apical aptency
    • In Gp A, apical patency will be maintained till obturation using electronic apex locator confirmed radiographically
  • Active Comparator: Non-apical patency
    • in Gp B apical patency will not be maintained

Clinical Trial Outcome Measures

Primary Measures

  • postoperative pain intensity using numerical rating scale
    • Time Frame: after 6 hours after root canal treatment
    • postoperative pain after root canal treatment
  • postoperative pain intensity using numerical rating scale
    • Time Frame: after12 hours after root canal treatment
    • postoperative pain after root canal treatment
  • postoperative pain intensity using numerical rating scale
    • Time Frame: after 24 hours after root canal treatment
    • postoperative pain after root canal treatment
  • postoperative pain intensity using numerical rating scale
    • Time Frame: after 48 hours after root canal treatment
    • postoperative pain after root canal treatment

Participating in This Clinical Trial

Inclusion Criteria

  • •1. Patient age between 18-60 years old. – 2. Both males and females will be included. – 3. All patients are in a good health without systemic condition. – 4. The offending tooth is a molar. – 5. The offending molar is indicated for root canal treatment. – 6. One molar for every patient. – 7. All patients will sign an informed consent. Exclusion Criteria:

  • 1. The offending tooth has previous attempt of pulp therapy or root canal treatment. – 2. The patient showing any clinical or radiographic evidence of periapical pathosis. – 3. Patients received analgesics or systemic antibiotic prior to treatment. – 4. Immunocompromised patients. – 5. Any unknown infectious disease (e.g. HBV, HCV, HIV, or T.B.) – 6. History of cancer with radio or chemotherapy. – 7. Offending molar with mobility score ≥2. – 8. Offending molar with pocket depth ≥6mm. – 9. Immature molars. – 10. Nonodontogenic pain. – 11. Patients with more than one tooth requiring endodontic intervention.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 60 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Cairo University
  • Collaborator
    • Zagazig University
  • Provider of Information About this Clinical Study
    • Principal Investigator: Heba Elasfouri, Associate professor – Cairo University
  • Overall Official(s)
    • Heba A ElAsfouri, AssProfessor, Study Director, Cairo University

References

al-Omari MA, Dummer PM. Canal blockage and debris extrusion with eight preparation techniques. J Endod. 1995 Mar;21(3):154-8. doi: 10.1016/s0099-2399(06)80443-7.

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