Status:
UNKNOWN
Analgesic Effect of Anahil and Ibuprofen on Pain After Root Canal Therapy in Patients With Pulpitis of the Molars in Qazvin(a City in Iran)
Lead Sponsor:
Qazvin University Of Medical Sciences
Conditions:
Irreversible Pulpitis
Eligibility:
All Genders
20-40 years
Phase:
PHASE2
Brief Summary
Hypothesis: 0: The analgesic effect of Ibuprofen and Anahil would be the same in reducing the pain after root canal therapy. 1: Ibuprofen shows higher potency to reduce the pain after root canal the...
Detailed Description
Patients will be selected from those who are referred to receive root canal therapy for the mandibular first molars with irreversible pulpitis. The current research and all the procedures will be don...
Eligibility Criteria
Inclusion
- Patients report spontaneous pain of the first molar of mandible ranging from 50 to 100 mm on a VAS (0-100 mm)
- The dental pulp's condition is irreversible pulpitis and the tooth is reparable and need the root canal therapy
- No evidences of any lesions and lucency, PDL widening, loss of lamina dura in radiographic examination
- Patients aged 20 to 50 years from both genders
- Patients are not pregnant or breast-feeding
- Healthy periodontal status (no evidences of aggressive/chronic periodontal diseases)
- No history of any systemic diseases (specially gastrointestinal and coagulation disorders)
- No history of allergic reaction to food nutrients (specially pineapple, celery, carrot, and fennel), NSAIDs and lidocaine
- No history of consuming the drugs interfere with NSAIDs, lidocaine and anticoagulants
- No use of other analgesic drugs within the last 6 hours
- Existence of no large restorations or crowns in treated tooth
- patients have no extreme fear of dental procedure
- Teeth with no evidence of infection or sinus tract
- Patients did not a previous RCT
Exclusion
- Patients who leave the study because of any reasons
- Special anatomy of teeth (extra canals, severe root curvature, calcifications, open apex, C shape, fractures,..)
- Patients who are not able to tolerate the single-session treatment (time, tooth's situation,..)
- If the aspiration through IAN block injection is positive
- If the diagnosis of pulp status has changed to partial necrosis during access cavity preparation
Key Trial Info
Start Date :
May 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2022
Estimated Enrollment :
72 Patients enrolled
Trial Details
Trial ID
NCT05349929
Start Date
May 1 2022
End Date
December 1 2022
Last Update
April 27 2022
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