Status:
COMPLETED
Effect of Preoperative Tramadol and Naproxen Sodium on Post Operative Pain
Lead Sponsor:
Dow University of Health Sciences
Conditions:
Symptomatic Irreversible Pulpitis
Post Operative Pain
Eligibility:
All Genders
18-60 years
Phase:
PHASE2
PHASE3
Brief Summary
The goal of this clinical trial is to compare in Tramadol, Naproxen sodium and Placebo in participants presenting with irreversible pulpitis in their mandibular posterior teeth. The main question\[s\...
Detailed Description
The adult participants who report in out-patient department (OPD) of Operative Dentistry at Dow International Dental College with the symptoms of irreversible pulpitis will be screened for the partici...
Eligibility Criteria
Inclusion
- ASA I and ASA II individuals who are between the ages of 18 and 60 years.
- Patients who have been diagnosed with symptomatic irreversible pulpitis (with either a normal periapex or symptomatic apical periodontitis).
- Patients who score moderate to severe (4-10) on a preoperative visual analogue scale (VAS= 1-10).
- Mandibular permanent premolar and molars.
Exclusion
- Patients who had taken painkillers or narcotics in the previous 12 hours
- Patients suffering from severe pain because of traumatic occlusion.
- Teeth with extensive damage, calcified canals, root resorption, and an open apex.
- Previously root canal treated teeth.
- Medically compromised patients (ASA-III and above)
- Those with special communication needs or who do not understand Urdu or English language.
- Pregnant and lactating women
- Individual patients who will be driving back alone
- Patients who are allergic to the prescribed medicines
Key Trial Info
Start Date :
March 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 15 2023
Estimated Enrollment :
47 Patients enrolled
Trial Details
Trial ID
NCT05982392
Start Date
March 1 2023
End Date
August 15 2023
Last Update
August 7 2024
Active Locations (1)
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1
Dow International Dental College
Karachi, Sindh, Pakistan, 75500