CTRI/2024/05/067948Not yet recruitingPhase 2
Comparative Evaluation of Post-Operative Pain usingContinuous and Reciprocating Motion Rotary File Systems - AClinical Trial - NI
ITS Dental College Hospital and Research Centre0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Vital teeth indicated for intentional RCT.
- •2. Age group- 20-50 years.
- •1. Single or multi rooted teeth (radiographically and clinically assessed).
- •2. Patients with completely formed roots(mature apex).
- •3. Teeth with only Vertucci Type 1 root canal morphology. Patients consenting to be a part of this study:
- •5. Medically fit patients (i.e no general
- •disease or pregnancy).
Exclusion Criteria
- •1. Teeth with wide or open apex
- •2. Non vital teeth.
- •3. Endodontic retreatment cases.
- •4. Third molars
- •5. Patients using analgesics, NSAIDs oranxiolytics during 7 days before the procedure.
- •6. Teeth with poor prognosis.
- •7. Teeth with complex root canal morphology.
- •8. Patients unwilling to participate in the study
- •9. Patients with active pain in any tooth.
- •10. Pregnant patients and nursing mothers. Presence of systemic diseases such as cardiovascular disease, renal disease and any bleeding disorders.
- •11. Patients with sinus tract, periapical abscess or facial cellulitis, known allergies or any contraindication to opioid or non-opioid analgesics including aspirin or NSAIDs.
- •12. Patients with known allergy to local anesthesia, sodium hypochlorite and chlorhexidine.
- •13. Presence of systemic diseases such as cardiovascular
- •disease,diabetes mellitus, renal disease and any bleeding disorders.
Investigators
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