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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
Use of newly introduced bioceramic putty in partial pulpotomy
Faculty of Dentistry, October 6 University
Giza, Egypt
Post operative pain
Measure intensity of post operative pain using visual analogue scale (VAS)
Time frame: after 24 hours
Post operative pain
Measure intensity of post operative pain using visual analogue scale (VAS)
Time frame: after 48 hours
Post operative pain
Measure intensity of post operative pain using visual analogue scale (VAS)
Time frame: After 72 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.