Efficacy of two medicaments in pain response and bleeding status in lower molars.
Phase 4
Completed
- Conditions
- Health Condition 1: 8- Other ProceduresHealth Condition 2: null- Patients with a clinical diagnosis of irreversible pulpitis in mandibular molars
- Registration Number
- CTRI/2018/07/014758
- Lead Sponsor
- aomi Ranjan Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Patients with clinical diagnosis of irreversible pulpitis in mandibular molars, i.e, participants experiencing moderate to severe pain even after administration of local anaesthesia and exhibiting a positive response to the electric pulp test and cold test with Endo-ice.
Exclusion Criteria
1.The subjects who are under medication that would alter pain perception as determined by oral questioning and written questionnaire.
2.Presence of any periapical pathology on radiographs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in pain during the subsequent endodontic procedureTimepoint: After 24 hours.
- Secondary Outcome Measures
Name Time Method Reduction in bleeding during the subsequent endodontic procedureTimepoint: After 24 hours.