Health Condition 1: M268- Other dentofacial anomalies
Conditions
Interventions
Intervention1: 4% Articaine: After obtaining the informed consent from the parents, 80 subjects would be randomly divided into two groups. Group 1 would constitute the 4% articaine group, while Group
Sponsors
Military Dental Centre
Eligibility
Inclusion criteria
Inclusion criteria: 1. Irreversible pulpitis wrt 16,17,18,26,27,28 indicated for extraction 2. Moderate to severe spontaneous pain
Exclusion criteria
Exclusion criteria: 1. Allergies to local anaesthetics or sulphites 2. History of significant medical conditions 3. Intake of any medications 4. Presence of abscess, sinus opening
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study will be the success rate of 4% lignocaine and 4% articaine anesthesia in surgery after a period of 15 minutesTimepoint: After 15 minutes of delivery of local anaesthesia | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome variables that could interpret the primary outcome are pinprick test pain score, anesthetic injection pain, intra-operative pain scores at every step of the surgical procedure, immediate post-operative pain, need for additional anesthesia, the total volume of LA used and patientsâ?? satisfaction with the anesthetic. Thus, these outcome variables will be measured and compared in this studyTimepoint: Visual analogue scale in all the outcomes after 15 minutes of delivering the local anaesthetic solution | — |
Countries
India
Contacts
Public ContactBudhaditya Paul
Indian Army
Outcome results
None listed