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Post Operative Pain of Partial Pulpotomy Using a Bioceramic Material in Patients With Symptomatic Irreversible Pulpitis

NCT05956613 EARLY_PHASE1 COMPLETED

The goal of this clinical trial is to assess post-operative pain of partial pulpotomy using a newly introduced Bioceramic material in young patients with symptomatic irreversible pulpitis at 24, 48, 72 hours postoperatively using visual analogue scale (VAS). The main question\[s\] it aims to answer are: • In patients with symptomatic irreversible pulpitis does the use of bioceramic material in partial pulpotomy decrease amount of post operative pain in comparison to conventional root canal treatment? Participants will record the intensity of pain at 24,48, 72 hours postoperatively.

Details

Lead sponsorOctober 6 University
PhaseEARLY_PHASE1
StatusCOMPLETED
Enrolment40
Start dateTue Aug 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionSun Oct 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Egypt