Clinical Trials Directory

Trials / Completed

CompletedNCT02981693

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
Phase
N/A
Study type
Interventional
Enrollment
283 (actual)
Sponsor
Hui Chen · Academic / Other
Sex
All
Age
12 Years – 80 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDURERoot canal sealerPatients 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.

Timeline

Start date
2014-01-01
Primary completion
2016-11-01
Completion
2016-11-01
First posted
2016-12-05
Last updated
2016-12-05

Source: ClinicalTrials.gov record NCT02981693. Inclusion in this directory is not an endorsement.