Laser therapy to reduce post endodontic pain in primary teeth
Not yet recruiting
- Conditions
- Other Procedures, (2) ICD-10 Condition: K040||Pulpitis,
- Registration Number
- CTRI/2023/04/051873
- Lead Sponsor
- Mohammed Salman Ali
- Brief Summary
This study is a randomized, parallel group, single centre trial comparing the post endodontic pain and frequency of analgesic intake after low level laser therapy in patients with symptomatic irreversible pulpitis in primary molars will be conducted at Bapuji Dental College and Hospital, Davangere, Karnataka, India. Single visit pulpectomy will be carried out for each individual followed which in intervention group low level laser therapy will be given and in control group no laser therapy will be given. Patients will be evaluate at 24 hours and 48 hours for post endodontic pain and frequency of analgesic intake.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 36
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 intake evaluation of post endodontics pain and frequency of analgesic intake at 24 hours and 48 hours postoperatively.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Bapuji Dental College and Hospital
🇮🇳Davanagere, KARNATAKA, India
Bapuji Dental College and Hospital🇮🇳Davanagere, KARNATAKA, IndiaMohammed Salman AliPrincipal investigator9066454214salmanali458@gmail.com