Comparative evaluation of efficiency oftransdermal patches of ketoprofen and diclofenacsodium with oral diclofenac tablet on postendodontic pain reduction following single visitroot canal therapy in symptomatic irreversiblepulpitis- A Randomized Clinical Study. ?

DR PRIYA PORWA0 sites78 target enrollmentTBD

Overview

No summary available.

Registry

who.int

Start Date

TBD

End Date

October 26, 2022

Last Updated

2 years ago

Study Type

Interventional

Sponsor

DR PRIYA PORWA

•Patients complaining of pain in anterior or single\-rooted premolar teeth of either jaw
•and diagnosed as symptomatic irreversible pulpitis with or without apical periodontitis
•having pre operative moderate to severe pain indicated for single visit endodontics will
•be included in the study.
•A written informed consent will be taken from all the patients and only those patients
•ready to sign the consent letter will be included in the study

•1\. Patients with known hypersensitivity against ketoprofen or diclofenac sodium will be excluded from the study.
•2\. patients with history of allergic reactions such as bronchospasm, shock, urticarial,
•etc., following the use of non\-steroidal anti\-inflammatory drugs (NSAIDs) will be excluded from the study.
•3\. Patients with high blood pressure and cardiac conditions will be excluded from the study.
•4\. Patients with sinus drainage, pus discharge, acute or chronic apical abscess will be excluded from the study.
•5\. Intentional RCT, fractured tooth having cracks or resorption will be excluded from
•6\. Patients with active stomach or duodenal ulceration within the last 6 months will be excluded from the study.
•7\. Patients undergoing treatment with other NSAIDs or corticosteroids during the
•study period will be excluded from the study.
•8\. Patients with developmental anomalies, congenital defects, pathology or open apex,