To test the Efficacy of two anesthetic agents in patients with pulpal pai
Phase 4
Completed
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2023/12/060698
- Lead Sponsor
- DR Paluru Harika
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
Healthy patients over 18 years old who had mandibular molars in need of root canal treatment in both the quadrants with irreversible pulpitis
Exclusion Criteria
Presence of systemic disorders
Sensitivity to lidocaine with 1:80,000 epinephrine
Presence of a periapical radiolucency
Lactating and pregnant women
Using any type of analgesic medication in the Preceding 12 hours before the treatment
Teeth that were unsuitable for restoration,with full crowns
Teeth associated with spontaneous severe pain that needed emergency treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate Anesthetic efficacy of Ropivacaine <br/ ><br>and Lidocaine using visual analog scale. <br/ ><br>Timepoint: 20 min after L.A During access cavity preparation ( entering in to dentin , pulp chamber) & instrument inserted in to the root canal.
- Secondary Outcome Measures
Name Time Method To evaluate the success rate of lidocaine and <br/ ><br>Ropivacaine using cold test <br/ ><br>Timepoint: 15 mins before & after giving local anesthesia <br/ ><br>