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Evaluation of iRoot SP as Root Canal Sealer: A Clinical Study

1-year Evaluation of iRoot SP as a Root Canal Sealer Compare to AH Plus Sealer: A Prospective Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02981693
Enrollment
283
Registered
2016-12-05
Start date
2014-01-31
Completion date
2016-11-30
Last updated
2016-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apical Periodontitis, Irreversible Pulpitis

Brief summary

The purpose of this study was to evaluate the clinical and radiological outcomes of iRoot SP as a root canal sealer in comparison with AH Plus sealer within 1-year follow up.Patients needing root canal treatment were enrolled and allotted into either iRoot SP group or AH Plus arm randomly. After root canal shaping and cleaning, the teeth were obturated according to their arms. Assessment of postoperative pain was done 1 week after root canal obturation using visual analog scale. After 1-year follow-up, clinical and radiographic evaluations were carried out. Statistical analysis at P \< 0.05 was conducted to measure difference between the arms.

Interventions

PROCEDURERoot canal sealer

Patients who required root canal therapy were enrolled and allotted into either iRoot SP arm or AH Plus arm randomly.For Test Arm: iRoot SP was used as a sealer. Obturation was performed with Gutta-percha cones and root canal sealer by continuous-wave condensation technique. For Control Arm: AH Plus was used as root canal sealer. The same steps were followed for obturation as in Test Arm.

Sponsors

Hui Chen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Subjects were required to: 1. have a mature tooth with closed apices; 2. have one single or multi-rooted tooth with irreversible pulpitis, pulp necrosis or apical periodontitis; 3. be prepared to appear for follow-up and 4. sign informed consent form.

Exclusion criteria

Subjects with: 1. moderate or severe marginal periodontitis; 2. internal or external root resorption in periapical radiograph; 3. active systemic disease; 4. physical or mental disability, 5. pregnant or lactating

Design outcomes

Primary

MeasureTime frameDescription
Radiographical assessments1 year after root canal therapyThe periapical status was assessed in the radiographs.Teeth with complete restitution of the periodontal contours were judged as healed. Teeth with a clearly decreased size of the periapical radiolucency were judged as healing. Teeth with unchanged, increased, or new periapical radiolucency were judged as failed.

Secondary

MeasureTime frameDescription
Clinical assessments1 year after root canal therapyThe root filled tooth was considered clinically successful if there was absence of clinical sign or symptom such as spontaneous pain, sensitivity to percussion or palpation, abnormal mobility, signs of pathology like abscess or sinus tract.
Postoperative Pain Evaluation1 week after root canal therapyPain was evaluated by using a visual analogue scale (VAS) made of a 10 cm line, where 0 = no pain and 10 = unbearable pain.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026