Clinical Performance of AH Plus Jet® Root Canal Sealers in Single-cone Protocols
Dentsply Sirona Implants and Consumables · NCT07642284
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 130
- US sites recruiting
- 1
- Study start
- September 9, 2026
- Record last updated
- September 11, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: AH Plus Jet® Endodontic Sealer; AH Plus Jet® Root Canal Sealing Material
Conditions: Root Canal Treatment
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Adult aged 18-75 at time of informed consent.
- Subject willing to participate in the clinical investigation and able to understand the content of the clinical investigation.
- Subject willing to return for follow-up visits.
- Subject has signed and dated the informed consent form.
- Subject in need of one or two primary root canal treatment on mature permanent anterior (incisor or canine) or premolar tooth.
- Planned study tooth has a favorable prognosis for the next 2 years.
Exclusion Criteria
- History of allergic reaction to epoxy resins or amines or any of the other product components.
- Subject has significant systemic health issues or chronic conditions (American Society of Anesthesiologists (ASA) class 3-6).
- Known pregnancy or is breastfeeding at time of enrolment or at the RCT visit.
- Subject unlikely to comply with investigational procedures, as judged by the Investigator.
- Sign of sinus tract or gingival swelling in the planned study position.
- Previous enrolment in the present clinical investigation.
- Involvement in the planning and conduct of the clinical investigation (applies to both Dentsply Sirona personnel and the clinical investigation site).
- Participation in another clinical investigation that may interfere with the present clinical investigation.
- Subject experiencing an intraoperative condition that may interfere with the evaluation of the investigational root canal sealer.
Recruiting US locations
New York University College of Dentistry
New York, NY 10010
Site contact: Matthew Malek
Study contacts (from the official record)
- Mikaela Friberg · +46 702 644 357 · mikaela.friberg@dentsplysirona.com
- Ulrika Bonander · +46 706 440 844 · ulrika.bonander@dentsplysirona.com