Group B: patients will be given prednisolone 20mg as premedication
DrugGroup B: patients will be given prednisolone 20mg as premedication
NCT Number: NCT07281807
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.
Trial opening soon.
Get Notified18 year–40 year
All sexes
Interventional
Phase 4
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Group B: patients will be given prednisolone 20mg as premedication
Group A: patients will be given piroxicam 20mg as premedication
Time frame: 48 hours
pain score on visual analogue scale
Contact information is provided by the study sponsor or research team.
RANA AHMAD
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06821763
Apical Periodontitis, Irreversible Pulpitis with Apical Periodontitis
Rawalpindi, Punjab Province, Pakistan
View Trial DetailsNCT07270159
Irreversible Pulpitis with Apical Periodontitis, Neurologic Manifestations
Karachi, Sindh, Pakistan
View Trial DetailsNCT07124962
Irreversible Pulpitis with Apical Periodontitis
Rawalpindi, Punjab Province, Pakistan
View Trial DetailsNCT07125911
Irreversible Pulpitis with Apical Periodontitis
Rawalpindi, Punjab Province, Pakistan
View Trial Details