se of a smaller needle or topical ice for reducing pain during local anesthesia in dental treatment
Not Applicable
- Conditions
- Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified
- Registration Number
- CTRI/2019/08/020545
- Lead Sponsor
- Manipal College of Dental Sciences Manipal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Includes healthy patients requiring bilateral maxillary first or second premolar extractions.
Exclusion Criteria
Excludes patients with diabetes, bleeding disorders, handicap, chronic pain conditions, any periapical pathology, who need premedication, nitrous oxide/oxygen sedation,
emergency cases, uncooperative patients, exceedingly anxious and those with any
history suggestive of being medically compromised
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective evaluation of pain is done 5 mins after each injection by Visual Analog Scale <br/ ><br>(VAS) by patient. Score 0 implies no pain or discomfort and Score 10 implies maximum pain or <br/ ><br>discomfort. <br/ ><br>Objective evaluation such as tingling sensation and numbness is evaluated after 5 mins.Timepoint: Subjective evaluation of pain - 5 mins after injection. <br/ ><br>Objective evaluation - 5 mins after injection.
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil