A clinical trial to study the pain induced during injection of local anesthesia
Not Applicable
Completed
- Registration Number
- CTRI/2020/12/029561
- Lead Sponsor
- Dr Arunajatesan Subbiya MDS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Healthy human volunteers -Adult males / females
Age : 25 to 40 yrs
Sex : Male and female
No systemic disease
No use of analgesics, sedatives, or anti-anxiety medications for at least 2 weeks before the study
Presence of an intact or minimally restored maxillary central incisor
No tenderness to percussion and palpation.
The diagnosis of a clinically normal pulp confirmed by the electric pulp test.
Exclusion Criteria
Pregnancy
Presence of systemic disease, medically compromised patients
Presence of sensitivity to lidocaine or dibucaine
Presence of deep carious lesion involving pulp of maxillary central incisor
Tenderness to percussion and palpation present
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Degree of pain during injection in a scale of 0 to 10Timepoint: 1-immediate <br/ ><br>2-after 24 hrs
- Secondary Outcome Measures
Name Time Method Degree of pain after 24 hrs of injection in a scale of 0to10Timepoint: 24hrs