N/A
N=160
Comparative Evaluation of Post-endodontic Pain Using Two Rotary Instrumentation Systems
Pain
Bottom Line
View on ClinicalTrials.gov: NCT02621034 ↗Enrolled (actual)
160
Serious AEs
—
Results posted
Jun 2016
Primary outcome: Primary: Post-operative Pain on the Visual Anlogue Scale (VAS) at the 6-hour Post-operative Interval — 5; 3.2; 3.5 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Control (Procedure); Reciproc (Procedure); One shape (Procedure)
- Age
- Adult · 20+ yrs
- Sex
- All
- Sponsor
- Zahedan University of Medical Sciences
- Primary completion
- Feb 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Post-operative Pain on the Visual Anlogue Scale (VAS) at the 6-hour Post-operative Interval |
5; 3.2; 3.5 | — |
| PRIMARY Comparison of Post-operative Pain in the Reciproc and Oneshape Groups Through Out the Intervals |
0.46; 0.34 | — |
| PRIMARY Comparison of Post-operative Pain Between the Three Groups at the 72-hour Interval |
0.72; 0.46; 0.34 | — |
Summary
In this study the investigators aim to compare the post-operative pain using two single-file endodontic rotary systems : Reciproc and One shape.
Eligibility Criteria
Inclusion Criteria
- Systematically healthy patients
- First or second molars with irreversible pulpitis without periapical pathosis.
- Single visit endodontic treatment
Exclusion Criteria
- Root canal retreatment
- Pregnancy
- The presence of a difficult root canal anatomy
- Internal or external resorption
- Teeth with open apices
- Any accident of complication occurred during treatment
- Presence of periapical lesion, abscess or sinus tract
Data sourced from ClinicalTrials.gov (NCT02621034). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.