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Comparison of Anesthesia Success Rate in Mandibular Inflammatory Tooth Between two Different Injection Techniques

Not Applicable
Conditions
tooth with irreversible pulpitis.
Pulpitis: NOS acute chronic (hyperplastic)(ulcerative) irreversible reversible
Registration Number
IRCT2013022712634N1
Lead Sponsor
Vice chancellor for research, Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

1) Patients with at least one posterior mandibular tooth with irreversible pulpitis for pulp therapy that each pulp therapy would be appliable thoroughly in one visit;
2) No history of taking any medication that would alter the inflammatory response of the pulp or provide analgesia for the previous 14 days;
3) No history of major systemic or cardiovascular disease;
4) Patients aged 18 to 65 years old;
5) Absence of acute inflammation and advanced periodontal disease at the injection area;
6) Provision written informed consent;
Exclusion criteria:
1) Any history of alergy to anesthetic solutions;
2) lack of cooperation or interest of patient to continue the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Success of the Anesthesia. Timepoint: After the Injection and during root canal therapy (RCT). Method of measurement: Vitality pulp test (pulp tester and endo ice) before RCT and questioning from patients during RCT.;Pain. Timepoint: During injection of Anesthetic solution. Method of measurement: Heft-parker visual Analogue Scale.;Blood Pressure. Timepoint: Before and After Anesthetic injection. Method of measurement: Digital indicator -mmhg.;Onset of Anesthesia. Timepoint: After the injection with 1-minute intervals for a period of 15 minutes. Method of measurement: Vitality pulp test (pulp tester and endo ice).;Duration of Anesthesia. Timepoint: From the beginning to the end of RCT. Method of measurement: Asking from the patients.
Secondary Outcome Measures
NameTimeMethod
Hematoma. Timepoint: One hour after the injection. Method of measurement: Observation.
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