About this trial
To compare the post operative mean pain scores by administering single-dose preoperative piroxicam and prednisolone in patients of irreversible pulpitis with symptomatic apical periodontitis.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Healthy patient ranging between 18-40 years
Having at least one premolar with diagnosis of symptomatic irreversible pulpitis according to history, examination and radiographs.
Teeth having mature apex confirmed by periapical radiographs.
Disqualifiers
History of systemic disorders including HIV, Hepatitis
Pregnancy (As per Medical record/ Verbally)
Patient using medication such as analgesics or anti-inflammatory drugs
Patient allergic to lignocaine, piroxicam and prednisolone
Trial design
Single group
Treatments tested in this trial
Group B: patients will be given prednisolone 20mg as premedication
DrugGroup B: patients will be given prednisolone 20mg as premedication
piroxicam 20mg
DrugGroup A: patients will be given piroxicam 20mg as premedication
Treatment groups
Trial outcomes
Primary outcomes
pain after single visit root canal treatment
pain score on visual analogue scale
Locations
Sponsors and contacts
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RANA AHMAD
Lead sponsor
Shaheed Zulfiqar Ali Bhutto Medical University
Sponsor institution
This trial is not recruiting at the moment. You can still explore other options: