Health Condition 1: K025- Dental caries on pit and fissure surface
Conditions
Interventions
Intervention1: 2% lidocaine at 20C: The patients shall receive buccal infiltration of the anesthetic solution near the maxillary first molars using 1.8 mL of 2% lidocaine (at 20�°C).
Control Interve
Sponsors
Faculty of Dentistry self funded
Eligibility
Inclusion criteria
Inclusion criteria: The subjects shall be in good health and none shall be taking any medication that would alter pain perception, as determined by oral questioning and written questionnaire. All test and control teeth shall not have any caries, large restorations, periodontal disease, endodontic treatment, and history of trauma or sensitivity.
Exclusion criteria
Exclusion criteria: Exclusion criteria will be known allergy or contraindications to any content of local anesthetic solution, patients who are pregnant or breast-feeding, a history of known or suspected drug abuse, and patients taking any drugs which could affect the pain perception. Patients having active pain in any teeth will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome shall be defined as the duration of pulpal anesthesiaTimepoint: Immediately after injection and after every 2 minutes, the teeth will be electric pulp tested, until no response to the maximum stimulus will be obtained. Duration of complete pulpal anesthesia will be defined as a period in which the subject had no response to maximal output of the pulp tester. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome shall be the onset of pulpal anesthesia.Timepoint: It shall be assessed immediately after the injection till complete pulpal anesthesia is obtained | — |
Countries
India
Contacts
Public ContactVivek Aggarwal
Jamia Millia Islamia
Outcome results
None listed