Viewing Study NCT06597487



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06597487
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: None
First Post: 2024-09-11

Brief Title: The Effect of Prognostic Factors on the Success of Full Pulpotomy in Permanent Mature Molars With Irreversible Pulpitis
Sponsor: None
Organization: None

Study Overview

Official Title: Influence of Wolters Classification of Pulpitis and the Radiographic Caries Depth Detected Using Artificial Intelligence on the Success of Full Pulpotomy in Permanent Mature Molars With Irreversible Pulpitis A Randomized Controlled Trial
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study aims to evaluate the effect of prognostic factors such as the degree of pulpal inflammation and the radiographic caries depth on the success of full pulpotomy in mature permanent molars with irreversible pulpitis
Detailed Description: Patients with mature permanent molars diagnosed with irreversible pulpitis will be enrolled in the study
The pre-operative pulpal status will be assessed using the American Association of Endodontists AAE classification and Wolters classification
Pre-operative radiographs will be taken and radiographic caries depth will be assessed
An Artificial Intelligence software will process the pre-operative X-rays to assess the presence of carious pulp exposure The diagnostic accuracy of the software will be evaluated by comparing its readings with clinical findings of pulp exposure after caries removal
The patients will be randomized to receive either full pulpotomy or conventional root canal treatment
The patients will be followed up for 1 3 and 6 months to assess clinical and radiographic success

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None