Health Condition 1: I10- Essential (primary) hypertension Health Condition 2: I10- Essential (primary) hypertension Health Condition 3: O- Medical and Surgical
Conditions
Interventions
Intervention1: 3% mepivacaine plain: 3%mepivacaine plain will be administered in controlled hypertensive and normal patients by inferior alveolar nerve block technique for 1 min.
Control Intervention1
Sponsors
Shanmugapriya K
Eligibility
Inclusion criteria
Inclusion criteria: 1. Able to provide informed consent. 2. Carious mandibular molars with diagnosis of symptomatic irreversible Pulpitis. 3. Patients who will be currently experiencing active pain in mandibular molars. 4. Participants should not be under any medications that would alter pain perception. 5. The patients should be clinically diagnosed with irreversible pulpitis, determined by spontaneous pain and prolonged response to cold testing with Endofrost (Coltene- Roeko) and a positive response to electric pulp testing, with absence of any periapical radiolucency on radiographs except for a mild widening of periodontal ligament space and a vital coronal pulp on access opening. 6. Every patient should have at least one opposing or contralateral molar without any deep coronal restoration, extensive caries, periodontal disease, which will be used as a control while pulp testing. 7. Blood pressure should be in the range of 120/80mm Hg to 160/100mm Hg.
Exclusion criteria
Exclusion criteria: 1. Allergies to local anaesthetics or sulphites. 2. Below the age of 18 years. 3. History of significant medical conditions. 4. Taking any medication, which may affect the pain assessment. 5. Active periapical pathosis. 6. Pregnant and Lactating women. 7. Mandibular molars without vital pulp tissue will be later excluded during endodontic procedures.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| efficacy of pulpal anesthesia with 3% mepivacaine and 2%lignocaineTimepoint: 3to 8mins after administration of the local anaesthesia and after each procedure the efficacy of the drug will be checked until the end of the procedure | — |
Secondary
| Measure | Time frame |
|---|---|
| onset of pulpal anesthesiaTimepoint: 2 mins after the administration of the local anesthesia, with electric pulp tester , onset will be determined . | — |
Countries
India
Contacts
Public ContactShanmugapriya K
RVS dental college and hospital
Outcome results
None listed