A study on the effect of two different concentration of pain reliever added to local anaesthesia agent in severe tooth pain condition.
Phase 3
- Conditions
- Health Condition 1: K029- Dental caries, unspecified
- Registration Number
- CTRI/2024/06/069566
- Lead Sponsor
- SRM Dental College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
•ASA I & II
•Pain severity with HP-VAS (85-170) Moderate – Severe in mandibular molars.
Exclusion Criteria
•ASA III
•Patient consumed any anti-inflammatory drugs 24 hrs before the day of reporting.
•Allergic to LA
•Pregnant & lactating women
•Patients under the influence of alcohol 24 hrs before the procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To comparatively assess the perioperative analgesic efficacy of 75 mcg and 150 mcg of buprenorphine with 2% lignocaine hydrochloride as a local anaesthetic agent in mandibular molars with symptomatic irreversible pulpitis and symptomatic apical periodontitis using heft-parker visual analogue scale.Timepoint: intraoperative and 6, 12, 24, 48 hrs post operative
- Secondary Outcome Measures
Name Time Method Pain experience assessmentTimepoint: intraoperative and 6, 12, 24, 48 hrs post operative