Health Condition 1: O- Medical and Surgical Health Condition 2: O- Medical and Surgical Health Condition 3: R52- Pain, unspecified
Conditions
Interventions
Intervention1: Administering Intra-osseous Injections: We will intervene the patients who has intra-operative pain during mandibular 3rd molar surgeries by administering intraosseous injections.
Contr
Sponsors
Self
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria were as follows: 1.Patients above 19 years of age, requiring surgical removal of impacted mandibular third molar. 2.Patients with pain while osteotomy at cancellous level during the procedure. 3.Patients with pain while splitting the tooth (odontectomy) or while luxating the tooth. 4.Patients who understood and were willing to follow all study protocols and who gave written consent.
Exclusion criteria
Exclusion criteria: 1.Patients below 19 years of age 2.Patients with severe infection 3.Patients with no pain while osteotomy of the bone at cancellous level or while splitting and luxating the tooth. 4.Patients with known allergies to local anesthetics (amides and esters) 5.Patients with other systemic diseases 6.Pregnant and lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the pain using VAPS (Visual Analog Pain Scale) intra-operatively at baseline, after administering Intra-osseous injections, 4week and 8 week after the procedure.Timepoint: To assess the pain using VAPS (Visual Analog Pain Scale) intra-operatively at baseline and after administering Intra-osseous injections, 4week and 8 week after the procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical complications will assessed at baseline and after 1 week.Timepoint: Clinical complications will assessed at baseline and after 1 week. | — |
Countries
India
Contacts
Public ContactJawahar Babu S
Sri Ramachandra Insititute of Higher Education and Research
Outcome results
None listed