Clinical Trials Directory

Trials / Completed

CompletedNCT05956613

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

Evaluation of Postoperative Pain After Partial Pulpotomy Versus Full Root Canal Treatment in Managing Young Permanent Molars With Symptomatic Irreversible Pulpitis: a Randomized Controlled Trial

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
40 (actual)
Sponsor
October 6 University · Academic / Other
Sex
All
Age
9 Years – 14 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREPartial pulpotomyUse of newly introduced bioceramic putty in partial pulpotomy

Timeline

Start date
2023-08-01
Primary completion
2023-10-01
Completion
2023-10-22
First posted
2023-07-21
Last updated
2024-05-14

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05956613. Inclusion in this directory is not an endorsement.

Post Operative Pain of Partial Pulpotomy Using a Bioceramic Material in Patients With Symptomatic Irreversible Pulpitis (NCT05956613) · Clinical Trials Directory