Post-endodontic pain.
Conditions
Interventions
Intervention 1: Intervention group: Potassium Diclofenac with the trade name of Cataflam from AMIN DARU production factory with the dose of 50 milligram in the format of 3 tablets are given to the pa
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: The tooth going to be treated, should be a maxillary or mandibular tooth The tooth going to be treated, should have asymptomatic irreversible pulpitis diagnosis Patients must be able to read, understand and reply the pain diagrams based on the Visual analogue pain scale Patients with informed consent could participate in the study Patients' physical situation should be in ASA1 group according to American anesthesia association
Exclusion criteria
Exclusion criteria: Patients using some drugs which interupt the prescribed drugs in the study If a patient has used any analgesic drugs, 12hours or less, before the root canal treatment If a patient has allergy to Non-steroidal anti inflammatory drugs(NSAIDs) Patients' pain be more than 40 in Visual analogue pain scale(VAS) before the treatment The root canal treatment can not be done in a single visit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The amount of root canal treated tooth's pain. Timepoint: Measurement of the scores of the patients' pain at 2, 4, 6, 12 and 24 hours after finishing of the root canal treatment. Method of measurement: Visual analogue scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSaba Salem
Shahid Beheshti University of Medical Sciences
Outcome results
None listed