CTRI/2024/05/067190Not yet recruitingPhase 4
A comparative evaluation of post-operative pain with Ultrasonic activation and laser irradiation using irrigation of 9 % etidronate & 2.5% NaOCl mixed solution in symptomatic irreversible pulpitis teeth A Randomized Clinical Study - NI
Dr Vinaya Pisal0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Healthy patients (Category: American Society of Anaesthesiologists class 1) (ASA House of Delegates 2014) aged between 18 – 60 years of age will be included.
- •2.maxillary or mandibular teeth diagnosed with Symptomatic irreversible pulpitis with or without periapical pathology or radiographic rarefaction.
- •3.Only those patients ready to sign the consent form will be included in the study.
Exclusion Criteria
- •1.Teeth with open apex, root resorption and calcified pulp chamber and canals will be excluded from the study.
- •2.Teeth with curvature more than 20 degree will be excluded from the study
- •3.patients taking analgesics 12 hours before the intervention.
- •4.Teeth which had received previous endodontic treatment will be excluded from the study.
- •5.Cases showing periodontal pockets deeper than 4mm will be excluded from the study.
- •6.Teeth with pre-op swelling, draining sinus and Flare ups during root canal treatment will be excluded from the study.
- •7.Any other iatrogenically affected root canal treatments will be excluded from the study.
- •8.Medically compromised patients will be excluded from the study.
Investigators
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