Pain Intensity After Root Canal Instrumentation
Not Applicable
Completed
- Conditions
- Pain, Postoperative
- Registration Number
- NCT04216940
- Lead Sponsor
- Ain Shams University
- Brief Summary
Assess the pain intensity in a two visit treatment of molars with irreversible pulpitis after instrumentation with two rotary systems Mpro and Hyflex files.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
- mandibular molars with acute pulpitis
Exclusion Criteria
- badly decayed non-restorable molars
- medically compromised patients
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Pain felt after mechanical instrumentation in the first visit up to 72 hours using Numeric Rating Scale (NRS) the participant will be asked to verbally rate their pain on a scale from 0 to 10, with 0 equal to no pain and 10 equal to worst possible pain
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie postoperative pain after root canal instrumentation in irreversible pulpitis cases?
How do MPRo and Hyflex rotary files compare to standard nickel-titanium systems in reducing postoperative dental pain?
Are there specific biomarkers that predict pain intensity following endodontic treatment with MPRo or Hyflex files?
What adverse events are associated with MPRo and Hyflex rotary instrumentation in molars with irreversible pulpitis?
How do MPRo and Hyflex rotary systems influence inflammatory cytokine profiles in postoperative irreversible pulpitis pain?
Trial Locations
- Locations (1)
Ain Shams University
🇪🇬Cairo, Egypt
Ain Shams University🇪🇬Cairo, Egypt