Trials / Unknown
UnknownNCT03488836
Evaluation the Post Operative Pain of Endodontic Treated Molar Tooth With Race and Reciprocal Systems Among Bandarabbas Patients in 2017
Evaluation the Post Operative Pain of Endodontic Treated Molar Tooth With Race and Reciprocal Systems Among Bandarabbas Patients in 2017: A Double Blind Randomized Controlled Trial
- Status
- Unknown
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 132 (estimated)
- Sponsor
- Sajad Ansari Fard · Academic / Other
- Sex
- All
- Age
- 20 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
extrusion of infected dentin into the periapical tissue has been suggested as a major source of pain after endodontic treatment. Although debris extrusion is an inevitable finding even when instrumentation is limited to the confines of the canal, different armamentarium seem to be associated with different amounts of debris extrusion. Studies on the effect of various rotary files on post-endodontic pain are very few and have yielded conflicting results with some favoring full-sequence and others leaning towards reciprocal rotary systems. This study aims at assessing the intensity of post-endodontic pain following two different rotary systems, Reciproc and race. Methods: in this single-blind, parallel-grouped randomized clinical trial a total of 150 otherwise healthy patients aged between 20 to 50 years old with a pulpal status of irreversible pulpitis for one tooth in the upper or lower molar region were analyzed. A clinician performed the endodontic treatment in two groups, a group instrumented using race and a third group with instrumentation performed using Reciproc rotary systems.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | reciproc | rotary reciprocating protocol |
| PROCEDURE | race rotary | race rotary group protocol |
Timeline
- Start date
- 2018-05-02
- Primary completion
- 2018-07-02
- Completion
- 2018-11-02
- First posted
- 2018-04-05
- Last updated
- 2018-04-05
Locations
1 site across 1 country: Iran
Source: ClinicalTrials.gov record NCT03488836. Inclusion in this directory is not an endorsement.