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Clinical Trials/CTRI/2024/06/068268
CTRI/2024/06/068268
Completed
Phase 4

Comparative evaluation of antimicrobial efficacy and Inter-appointment pain with 3% sodium hypochlorite at different intracanal temperatures in teeth with Pulp necrosis with Symptomatic Apical periodontitis- A Randomized Clinical Study - NI

Dr Shreya Volety0 sites45 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: K041- Necrosis of pulp
Sponsor
Dr Shreya Volety
Enrollment
45
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
August 7, 2024
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Dr Shreya Volety

Eligibility Criteria

Inclusion Criteria

  • Healthy patients (Category: American Society of Anesthesiologists class 1\) (ASA House of Delegates 2014\) aged between 18 – 60 years of age with teeth diagnosed with pulp necrosis with symptomatic apical periodontitis.
  • 2\. Necrotic pulps as confirmed by negative response to sensitivity pulp tests.
  • 3\. Teeth with symptomatic apical periodontitis
  • 4\. Teeth with or without periapical radiolucency size less than 2 mm.
  • 5\. A written informed consent will be obtained from all the patients and only those
  • Patients who are ready to sign the consent form will be included in the study

Exclusion Criteria

  • Patients suffering from a significant systemic condition.
  • 2\. Patients who received antibiotic therapy within the previous 3 months
  • 3\. Teeth with calcified pulp chamber
  • 4\. Teeth that had received previous endodontic treatment
  • 5\. Cases showing periodontal pockets deeper than 4mm.
  • 6\. Patients on medications such as chemotherapy, anticoagulants, corticosteroids,
  • bisphosphonates and immunosuppressant drugs

Outcomes

Primary Outcomes

Not specified

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