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Clinical Trials/NCT05763420
NCT05763420
Enrolling By Invitation
Not Applicable

Clinical Efficacy of AH Plus Bioceramic Sealer in Root Canal Treatment of Molar Teeth: A Randomized Controlled Trial

Ministry of Health, Kuwait1 site in 1 country136 target enrollmentAugust 7, 2023

Overview

Phase
Not Applicable
Intervention
AH Plus Bioceramic Sealer
Conditions
Root Canal Infection
Sponsor
Ministry of Health, Kuwait
Enrollment
136
Locations
1
Primary Endpoint
Assessment of clinical outcome by assessing the resolution/persistence/development of clinical signs and symptoms
Status
Enrolling By Invitation
Last Updated
3 months ago

Overview

Brief Summary

The goal of this clinical trial is to assess the efficacy and outcome of sealer-based obturation (SBO) using a new calcium silicate sealer in comparison with warm vertical compaction (WVC) using a resin-based sealer, which is the current gold standard.

Detailed Description

Calcium silicate sealers are used in endodontics because of their biocompatibility, bioactivity, and their ability to form a hydroxyapatite-mediated interfacial bond with root canal dentine. Although in vitro and retrospective clinical studies have reported promising findings, there remains a lack of prospective, well-controlled trials evaluating their clinical and radiographic performance. Aims and Objectives: 1. To compare the clinical outcome of single-cone bioceramic obturation (SBO) with warm vertical compaction (WVC) in primary root canal treatment. 2. To compare the radiographic outcome of SBO and WVC using periapical (PA) radiographs and cone-beam computed tomography (CBCT). Materials and Methods: Patients referred for primary root canal treatment of molar teeth at Jaber Al-Ahmed Dental Center who fulfil the inclusion and exclusion criteria will be invited to participate. Written informed consent will be obtained from all participants. Preoperative PA radiographs and CBCT scans will be taken. After completion of root canal instrumentation, participants will be randomly allocated to either Group A: SBO or Group B: WVC. Participants will be blinded to the obturation technique. Allocation will remain concealed until canals are ready for obturation, at which time the treating clinician will be informed of the assigned method. All teeth will receive definitive restorations following obturation. Participants will be recalled at 12 months for clinical and radiographic evaluation using PA radiographs and CBCT, and will subsequently be followed annually for up to 4 years. The study will conform to the CONSORT statement and will be conducted in accordance with the Declaration of Helsinki. Ethical approval has been granted by the local health authority (ID: 2291). Statistical and Analytical Plan: Sample size estimation for the primary healing outcome was performed using PASS (NCSS, Kaysville, UT, USA). Burns et al. (2022) reported pooled healing rates of approximately 92-93% under loose criteria and 82% under strict criteria in primary NSRCT, indicating that reductions on the order of 10-12 percentage points are clinically meaningful. Based on these data, an absolute 12% difference (0.99 vs 0.87) was considered clinically important. Using a two-sided test comparing two independent proportions, with 80% power and 5% significance level, detecting this 12% absolute difference required 108 teeth (54 per group). Accounting for a 20% anticipated loss to follow-up, the required sample size is 136 teeth (68 per group). Healing at 12 months will serve as the dependent variable in logistic regression models. Predictor variables will include age, sex, preoperative status, presence of apical periodontitis, preoperative pain, patency, apical preparation size, root filling quality, and sealer type. Two-way interactions will be assessed. Analyses will follow the intention-to-treat principle. Null Hypothesis: H₀: There is no difference between SBO and WVC in clinical or radiographic healing outcomes at 12 months.

Registry
clinicaltrials.gov
Start Date
August 7, 2023
End Date
January 29, 2027
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Aldowaisan

Principal Investigator, Specialist in Endodontics

Ministry of Health, Kuwait

Eligibility Criteria

Inclusion Criteria

  • Participants must be 18-65 years of age at the time of recruitment
  • Participants must have a classification of I or II on the American Society of Anesthesiologists (ASA) physical status classification system
  • Participants must not have known allergies to any materials used in the study
  • Participants must agree to participate in the study by signing a consent form
  • Participants must have good oral hygiene
  • Maxillary and mandibular permanent molar teeth that require primary root canal treatment will be included
  • The teeth must be restorable and have fully formed roots with no advanced periodontal disease

Exclusion Criteria

  • ASA classification of III or more
  • Pregnant or breastfeeding women
  • Patients who are unable to give consent
  • Patients who have advanced periodontal disease or teeth with more than 5mm probing
  • Anterior, premolar and third molar teeth
  • Teeth whose apices were over-enlarged at the time of pulp extirpation
  • Teeth with broken instruments
  • Teeth with blocked or non-negotiable canals
  • Teeth with iatrogenic perforations
  • Teeth with incomplete root formation

Arms & Interventions

SBO with AH Plus Bioceramic Sealer

The teeth will be obturated using a single cone technique with AH Plus Bioceramic Sealer.

Intervention: AH Plus Bioceramic Sealer

WVC with resin-based AH Plus Sealer

The teeth will be obturated using warm vertical compaction with resin-based AH Plus Sealer.

Intervention: AH Plus Sealer (resin-based)

Outcomes

Primary Outcomes

Assessment of clinical outcome by assessing the resolution/persistence/development of clinical signs and symptoms

Time Frame: Change from baseline at 12 months

The examiner will label the teeth as having a normal clinical outcome (absence of pain, swelling and other symptoms, no sinus tract, no loss of function) or showing signs and symptoms clinical outcome (the tooth is associated with signs and/or symptoms of infection).

Assessment of radiographic healing with cone beam computed tomography (CBCT) scans using Estrela's PAI (periapical index)

Time Frame: Change from baseline periapical lesion size at 12 months

Estrela's PAI based on CBCT will be used in logistic regression models with different predictor variables.

Study Sites (1)

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