Effect of buffered anesthetics in odontogenic infections

Phase 4

Registration Number: IRCT20230622058557N2

Lead Sponsor: Armed Forces Institute of Dentistry

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 70

Inclusion Criteria

Patient between 18 to 70 years that have Odontogenic maxillofacial infection surrounding any tooth.
Lack of sensitivity to local anesthetics
Patients having acute abscess of any tooth
Patients having acute periapical periodontitis leading to granuloma formation
Patients having physical status 1 and 2 according to American Society of Anesthesiologists(ASA) classification

Exclusion Criteria

Patients with systemic diseases for which injections of lignocaine with adrenaline are contraindicated will be excluded from the study
Anesthesia allergy or drug abuse history

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain Assessment: Pain will be determined by the patient before and after injection using VAS Pain score. It is a 10 cm long scale with 0 marking indicating no pain to 10 marking as worst pain possible. Timepoint: Before and immediately after local anesthetic injection. Method of measurement: Visual Analog Pain Score.;Efficacy of Anesthesia: Determined by the onset of anesthesia i.e. the first feeling of numbness in the region of the teeth anaesthetized checked by inserting straight probe in the gingival sulcus of the involved region. Timepoint: Immediately after injection is administered with 30 seconds intervals . Method of measurement: Seconds.

Secondary Outcome Measures