Comparative evaluation of Anesthetic Efficacy of needleless anesthesia and conventional anesthesia in patients with Symptomatic irreversible pulpitis. A Randomized Clinical Trial
Phase 2
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2021/12/038471
- Lead Sponsor
- Krishnakanth Jaju
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Pa1ents with symptoma1c irreversible pulpi1s
Exclusion Criteria
<18 years of age, medically compromised individuals, individuals with
periapical lesion, individuals allergic to local anesthesia, pregnant woman,alcoholics,drug users.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset, depth of anaesthesiaTimepoint: 15 minutes from time of injection
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil