Summary
A prospective, parallel-group, randomised, post-market clinical follow-up investigation evaluating the performance and safety of the modified formula of the AH Plus Jet® Endodontic Sealer (also referred to as ES) and the predicate AH Plus Jet® Root Canal Sealing material (also referred to as RCS). Around 150 teeth will be randomly assigned to receive either ES or RCS root canal treatment using the single-cone technique. A maximum of 2 teeth per participant will be included and "tooth" will be considered the statistical unit and hence considered independent even if the teeth are in the same participant. Participants will be followed up for a period of 24 months to assess the outcomes.
Eligibility Criteria
Age Range: 18 years to 75 years
Inclusion Criteria:
1. Adult aged 18-75 at time of informed consent.
2. Subject willing to participate in the clinical investigation and able to understand the content of the clinical investigation.
3. Subject willing to return for follow-up visits.
4. Subject has signed and dated the informed consent form.
5. Subject in need of one or two primary root canal treatment on mature permanent anterior (incisor or canine) or premolar tooth.
6. Planned study tooth has a favorable prognosis for the next 2 years.
Exclusion Criteria:
1. History of allergic reaction to epoxy resins or amines or any of the other product components.
2. Subject has significant systemic health issues or chronic conditions (American Society of Anesthesiologists (ASA) class 3-6).
3. Known pregnancy or is breastfeeding at time of enrolment or at the RCT visit.
4. Subject unlikely to comply with investigational procedures, as judged by the Investigator.
5. Sign of sinus tract or gingival swelling in the planned study position.
6. Previous enrolment in the present clinical investigation.
7. Involvement in the planning and conduct of the clinical investigation (applies to both Dentsply Sirona personnel and the clinical investigation site).
8. Participation in another clinical investigation that may interfere with the present clinical investigation.
9. Subject experiencing an intraoperative condition that may interfere with the evaluation of the investigational root canal sealer.