Assessment of Vital Pulp Therapy in Permanent Molars

Status Recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the long term clinical performance of vital pulp therapy of young permanent teeth with irreversible pulpitis

Clinical Trial Description

Permanent molar teeth meeting the inclusion criteria will be included into the study. Following local anaesthesia and dental dam application, caries excavation will be performed; and after exposure, the pulp will be amputated to the level of the canal orifices (full pulpotomy) using a sterile high-speed round bur under water coolant. After haemostasis is achieved, Mineral trioxide aggregate (MTA) will be gently placed over the pulp to a thickness of 2-3 mm and the tooth will be restored using glass ionomer cement and composite resin. A postoperative periapical radiograph will be taken. Patients will be reviewed at 6., 12., 24. and 36. months for clinical and radiographical success. The data will be analysed statistically using chi square test. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03410134
Study type	Interventional
Source	Hacettepe University
Contact	Zafer C Cehreli, Prof
Phone	00905353197969
Email	zcehreli@gmail.com
Status	Recruiting
Phase	N/A
Start date	November 1, 2017
Completion date	August 1, 2023

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