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NCT05726357 Clinical Trial

Pulpotomy vs Root Canal Treatment for Teeth With Symptomatic Irreversible Pulpitis

Pulpitis - Irreversible Clinical Trial

Official title:
Pulpotomy vs Root Canal Treatment for Teeth With Symptomatic Irreversible Pulpitis: A Randomised Control Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05726357
Other study ID # FD BUE REC 22-034
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date November 30, 2024

Study information
Verified date August 2023
Source British University In Egypt
Contact Shehabeldin Saber, phD
Phone +202 26890000
Email shehabeldin.saber@bue.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

high-quality evidence is needed to add to current knowledge and also assess the long-term outcomes for full/complete pulpotomy after carious pulpal exposure in patients with signs and symptoms indicative of irreversible pulpitis

Recruitment information / eligibility
Status Recruiting
Enrollment 380
Est. completion date November 30, 2024
Est. primary completion date March 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - a mature permanent tooth - symptoms indicative of IRP - responsive to cold and EPT sensibility testing - restorable and can be adequately isolated during treatment - One tooth (molar or premolar) per patient. Exclusion Criteria: - active periodontal disease - complex medical histories - unable to consent - pregnant or breast-feeding - excessive bleeding that cannot be controlled

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• vital pulp therapy
removal of the coronal pulp followed by placing a biocompatible material to preserve the vitality of the radicular pulp

Locations
Country Name City State
Egypt Faculty of Dentistry Cairo

Sponsors (1)
Lead Sponsor Collaborator
British University In Egypt

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain score score by a numeric rating scale from 1(minimum pain) to 100 (maximum pain) day 3 post treatment
Secondary pain score score by a numeric rating scale from 1(minimum pain) to 100 (maximum pain) 6 months post treatment
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