A novel maxillary injection technique to reduce the multiple injections
Phase 1
Completed
- Registration Number
- CTRI/2019/12/022215
- Lead Sponsor
- DrJArockia Antony Praveen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
1. Patients with age group of 18-70 years.
2. Patients with deep pockets (PPD>=5mm).
3. Patients who are undergoing Non-surgical periodontal therapies under local anaesthesia in maxilla.
4. Patients with ASA class â? and â?¡.
Exclusion Criteria
1. Patients under analgesic, anti-inflammatory, anti-depressive medications.
2..Patients who are allergic to any of the local anesthetic drug.
3. Pregnant and lactating women.
4. Patients with bleeding disorders , neurological disorders.
5.Patients with missing upper premolars.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. The perception of numbness of palatal and buccal tissues. <br/ ><br> 2. Numbness of one entire maxillary quadrant. <br/ ><br>3.VAS score on pain perception.Timepoint: The duration and perception of anaesthesia is noted on after 5, 10, 20, 30, and 60 minutes.
- Secondary Outcome Measures
Name Time Method 1.Pain on transgingival probing at one site in every tooth of the maxillary arch.(Pinprick test).Timepoint: The duration and perception of anaesthesia is noted on after 5, 10, 20, 30, and 60 minutes.