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Clinical Trials/CTRI/2022/09/045690
CTRI/2022/09/045690
Not yet recruiting
Phase 3

Effect of Resin-based and Bioceramic Root Canal Sealers on Postoperative Pain following Continuous Chelation- A Randomized Controlled Clinical Trial

SRM DENTAL COLLEGE0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: K040- Pulpitis

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: K040- Pulpitis
Sponsor
SRM DENTAL COLLEGE
Status
Not yet recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
SRM DENTAL COLLEGE

Eligibility Criteria

Inclusion Criteria

  • •1\. Good oral hygiene.
  • •2\. Patients belonging to ASA (American Society of Anesthesiologists) Category I and II.
  • •3\.Patients had not used any analgesic in last 7 days.
  • •4\. Patients had not used any antibiotic in last 7 days.
  • •5\. Patients diagnosed with symptomatic or asymptomatic irreversible pulpitis caused by deep carious lesion in the mandibular first or second molar teeth.
  • •6\. The presence of profusely pulp bleeding with a thick consistency, which is exposed during caries removing.
  • •7\. Patients who had healthy periapical tissues (confirmed with periapical radiography)

Exclusion Criteria

  • •1\. Patients who refuse to participate in this study.
  • •2\. Medically compromised patients (with immunosuppressive / systemic diseases, patients on medications).
  • •3\.Non\-vital teeth.
  • •4\. The presence of advanced periodontal disease (probing depth \> 4 mm).
  • •5\. The presence of open apex, presence of calcification, presence of resorption, root caries.
  • •6\. Patients who had multiple teeth requiring endodontic treatment.
  • •7\. Patients with allergic sensitivity to materials and agents that should be used during the root canal treatment.
  • •8\. Patients who had allergic sensitivity to local anesthetics.
  • •9\. Patients who had systemic or allergic sensitivty for the NSAIDs.
  • •10\. Pregnant patients and patients in lactation period.

Outcomes

Primary Outcomes

Not specified

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