CTRI/2020/04/024612
Not yet recruiting
未知
COMPARATIVE EFFICACY OF 2 INJECTION METHODS WITH ARTICAINE FOR TREATMENT IN MANDIBULAR MOLARS WITH SYMPTOMATIC IRREVERSIBLE PULPITIS. A CONSORT RANDOMIZED DOUBLE-BLIND CLINICAL TRIAL : AN IN-VIVO STUDY.
Dr Harsh Jain0 sites0 target enrollmentTBD
ConditionsHealth Condition 1: K040- Pulpitis
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: K040- Pulpitis
- Sponsor
- Dr Harsh Jain
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Systemically healthy patients.
- •2\. Patients 18â??65 years old.
- •3\. Not allergic to articaine or epinephrine.
- •4\. No facial paresthesia.
- •5\. Not taking any analgesic drug 6 hours before treatment.
- •6\. Not taking any medication that interferes with anesthesia, such as tricyclic antidepressants and beta\-blockers.
- •7\. The absence of pathogenesis in areas planned for injection.
- •8\. Not pregnant.
- •9\. The absence of pathologic periodontal pockets during probing.
- •10\. Patients with a mandibular molar tooth exhibiting symptomatic irreversible pulpitis.
Exclusion Criteria
- •1\. A standard inferior alveolar nerve block injection will be performed using articaine 4% with epinephrine 1:100,000\. Ten minutes after the injection, the patients will be asked about lip numbness. Patients without profound lip numbness will be excluded from the study because the block will be considered â??missedâ?? which will also be confirmed with electric pulp sensibility test.
- •2\. Participants with periapical lesions, abscesses or cellulites at the relevant tooth, those with a medical treatment history or those having undergone root canal treatment for the relevant tooth will also be excluded from the study.
Outcomes
Primary Outcomes
Not specified
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