None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient requiring extraction of Maxillary premolar. 2. Patients over age of 15 years, both male and female will be included in this study. 3. Systemically healthy patients. 4.Co-operative, motivated and hygiene conscious patients.
Exclusion criteria
Exclusion criteria: 1) Pregnant or lactating females. 2) Patient with periapical infection in maxillary premolars. 3) Allergy to any local anaesthetic agent and anti-inflammatory drugs. 4) Patients with high-risk systemic diseases. 5) Those who deny for consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The outcomes of this study will include the onset time, duration of anaesthesia, pain perception during the orthodontic extraction procedure, postoperative pain, analgesic consumption, patient satisfaction, and any adverse effects, to evaluate the efficacy and safety of adrenaline, clonidine, and dexmedetomidine as adjuvants to lignocaine in infraorbital nerve blocks.Timepoint: Outcome variables were assessed at predetermined time points, including onset of anaesthesia (30 seconds to 5 minutes post-block), duration of anaesthesia (until return of sensation), intraoperative pain during extraction, postoperative pain at 1, 2, 4, 6, 12, and 24 hours, analgesic consumption within 24 hours, patient satisfaction at 24 hours, and adverse effects monitored immediately, within 2 hours, and at 24 hours post-procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| NilTimepoint: Nil | — |
Countries
India
Contacts
Ranjeet Deshmukh Dental college and Research centre