In Vivo Study on the Material Properties of iRoot SP and nRoot SP Root Canal Sealers

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Dental Hospital of Zhejiang University School of Medicine

About this trial

A randomized controlled trial was conducted to compare the treatment efficacy of iRoot SP and nRoot SP Root Canal Sealer Materials in patients with chronic apical periodontitis.

Eligibility criteria

Qualifiers

Age ≥ 18 years.

Diagnosis of apical periodontitis conforming to the diagnostic criteria in Endodontics.

The affected tooth is deemed restorable upon evaluation, with non-vital pulp requiring extirpation.

The affected tooth is a single tooth with a fully developed apical foramen.

Disqualifiers

Patients with alveolar bone loss exceeding one-third of the root length.

Affected teeth with root fracture, root canal obstruction, calcification, or root surface caries.

Patients with severe systemic diseases (e.g., osteoporosis, mental disorders, hepatic or renal insufficiency).

Patients who have taken analgesics, immunosuppressants, or antibiotics within one week prior to enrollment.

Trial design

Treatments tested in this trial

  • iRoot SP
  • nRoot SP

Treatment groups

160 Participants
are divided into 2 treatment groups