Evaluating the pain at site, onset of action, duration and anesthetic efficacy of conventional, buffered lidocaine and precooled lidocaine.
Not Applicable
- Conditions
- Health Condition 1: K044- Acute apical periodontitis of pulpal origin
- Registration Number
- CTRI/2024/08/071805
- Lead Sponsor
- Shalini Reddy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
diagnosed with Symptomatic Irreversible Pulpitis with moderate to severe pain (preoperative pain score=4) as measured on visual analog scale (VAS) participated in this trial. Criteria for inclusion were patients from 18 to 45 years of age and belonging to ASA category classes I and II with SIP in mandibular molar
Exclusion Criteria
Patients who refused to give informed consent, allergic to local anaesthetics or any other drugs and/or conditions that influence the pain scores, and with presence of periapical radiolucency (other than a widened periodontal ligament), swelling, and sinus tract were excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anesthetic Efficacy <br/ ><br>Timepoint: Baseline scores, during and after treatment, after 3 hours
- Secondary Outcome Measures
Name Time Method Onset of action <br/ ><br>pain at site <br/ ><br>durationTimepoint: start of the procedure to 3 hours