se of soft laser for increasing success of inferior alveolar nerve block in symptomatic pulpitis.
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/12/060840
- Lead Sponsor
- DR SHAHNAZ
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 172
Healthy patients having a first or second mandibular molar tooth with symptomatic irreversible pulpitis and normal periapical radiographic appearance. The clinical diagnosis of symptomatic irreversible pulpitis will be confirmed by a response to an electric pulp and a prolonged exaggerated response (10 seconds) with moderate to severe pain to a cold test. One hundred twenty patients eligible to participate study will be included.
Presence of systemic disorders, a sensitivity to lidocaine with 1:80,000 epinephrine or to NSAIDs, nasal polyp, a history of gastrointestinal ulcers, lactation, pregnancy, using any type of analgesic medication in the preceding 12 hours before the treatment, having a tooth not suitable for restoration, and having a full crown.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method success of inferior alveolar nerve block by using Heft parker pain rating scale during root canal treatmentTimepoint: success of inferior alveolar nerve block by using Heft parker pain rating scale during root canal treatment
- Secondary Outcome Measures
Name Time Method post endodontic pain following root canal treatment.Timepoint: post operatively after 6, 12, 24 and 48 hrs after treatment