None listed
Conditions
Interventions
Intervention1: Precaine gel: Precaine gel (Lidocaine 8%, Dibucaine 0.8%) (Pascal Co Inc, Bellevue, WA, USA)
Control Intervention1: Placebo gel: water based gel
Sponsors
Dr Arunajatesan Subbiya MDS
Eligibility
Inclusion criteria
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
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
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Degree of pain after 24 hrs of injection in a scale of 0to10Timepoint: 24hrs | — |
Primary
| Measure | Time frame |
|---|---|
| Degree of pain during injection in a scale of 0 to 10Timepoint: 1-immediate 2-after 24 hrs | — |
Countries
India
Contacts
Public ContactDr Arunajatesan Subbiya MDS
Sree Balaji Dental college & Hospital
Outcome results
None listed