aser therapy to reduce post endodontic pain in primary teeth
Not Applicable
- Conditions
- Health Condition 1: 8- Other ProceduresHealth Condition 2: K040- Pulpitis
- Registration Number
- CTRI/2023/04/051873
- Lead Sponsor
- Mohammed Salman Ali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
symptomatic irreversible pulpitis in primary molars
- symptomatic pulpitis with spontaneous pain or lingered by cold or heat
- mobility less than 1
Exclusion Criteria
- absence of bleeding after pulpal exposure (necrotic teeth)
- no responds to cold and heat test
- lidocaine hypersensitivity
- children who have taken antibiotic or analgesic before 6 hrs of treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evaluation of post endodontics pain and frequency of analgesic intakeTimepoint: evaluation of post endodontics pain and frequency of analgesic intake at 24 hours and 48 hours postoperatively.
- Secondary Outcome Measures
Name Time Method nilTimepoint: nil