Post operative endodontic pain. Other specified disorders of teeth and supporting structures
Conditions
Interventions
Intervention 1: Interventional group: After inferior Alveolar injection and before the beginning of the treatment the primary group will receive an injection of 0.4 mL ( 0.2 mL in mesio buccal and 0.2
Treatment - Drugs
Interventional group: After inferior Alveolar injection and before the beginning of the treatment the primary group will receive an injection of 0.4 mL ( 0.2 mL in mesio buccal and 0.2 mL in disto buc
Control group: wil be injected with 0.4 mL of 2% Lidocain with EP 1/180000
Sponsors
Dental Azad University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: healthy (ASA I, II); Patients with first or second mandibular molars who need endodontic treatment; Vital tooth without a history of past endodontic treatment; Patients with clinical evidence of irreversible Pulpits with moderate to severe pain; Patients without pre apical lesion and periodontal ligament enlargement more than 0.75-1mm on the x-ray images; Patients in the age group of 18-65 years old. Exclusion criteria: Pregnant or nursing; necrotic tooth; Patients with allergy or contraindication toward non-opioid or opioid painkillers such as aspirin or NSAIDs; People who have a history of acute peptic ulcer, during the past 12 months; People who have bleeding problems or have been taking anticoagulant drugs over the past month; Patients who have taken opioid or non opioid or steroid pain killers, antidepressants or sedative drugs.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post oprative endodontic pain. Timepoint: 6-12-24-48 hours after treatment. Method of measurement: Visual Analogue Scale (VAS 0-9mm). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Peyman Mehrvarzfar
Endodontic department, Dental School of Tehran Azad University
Outcome results
None listed