Post-operative Pain With Different Apical Finishing Sizes After Single Visit Root Canal Treatment
NCT05847738 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25
Last updated 2023-05-08
Summary
This is a randomized controlled parallel clinical, prospective split mouth, triple blinded study. Sample size calculation was conducted and it was 25 subjects per group for a total of 50 sides to compensate for drop-outs.
Patient selection and preparation:
All root canal treatments were performed by a single endodontic consultant. All subjects were selected from walk in patients presented to the endodontic clinic of the British university in Egypt. Cases that met the inclusion criteria where selected for this study. All patients were verbally informed about the procedure's benefits and that the results of the treatment will be used to this study and the risks of the procedure was explicitly explained to them. After the verbal consent patients were handed a written form consent to sign upon.
All data of post-operative pain were recorded by a second blinded clinician through a visual analog scale (VAS). Post-operative monitoring periods will be recorded in 12 hours, 24 hours, 3 days and one week Data was sent to the statistician with group names only to fulfill the triple blinding criteria and results will be interpreted
Conditions
- Pain Assessment
Interventions
- BEHAVIORAL
-
Pain assessment
Pain was assesd postoperatively in both groups at time intervals
Sponsors & Collaborators
-
British University In Egypt
lead OTHER
Eligibility
- Min Age
- 25 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-03-15
- Primary Completion
- 2023-03-30
- Completion
- 2023-04-15
Countries
- Egypt
Study Locations
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