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RecruitingNCT07206108

Clinical Trial of Modified Endocrown and Personalized Post-core and Crown for Large-area Tooth Defects After Root Canal Treatment

A Multicenter, Randomized Controlled, Single-blind, Non-inferiority Clinical Trial of Modified Endocrown and Personalized Post Core Combined With Full Crown for Large-area Tooth Defects After Root Canal Treatment

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
246 (estimated)
Sponsor
Nanfang Hospital, Southern Medical University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study intends to adopt a multicenter, randomized controlled, single-blind, non-inferiority clinical trial design. 246 premolars that meet the inclusion criteria after complete root canal treatment will be selected from the clinical practice and randomly divided into two groups. One group will be restored with the modified endocrown, and the other group will be restored with personalized post and core combined with full crown. Follow-up visits were conducted at 6 months, 1 year and 2 years after the operation respectively. Through clinical and imaging examinations, the survival rates of the two different restorations were evaluated and used as the main evaluation indicators to fill the gap in efficacy data of the modified endocrown in clinical applications, providing a strong evidence-based medical basis for subsequent restoration improvement and standardized application.

Conditions

Interventions

TypeNameDescription
PROCEDUREmodified endocrownCombining the advantages of post-core crown and endocrown, an modified endocrown was designed

Timeline

Start date
2025-08-04
Primary completion
2029-12-31
Completion
2029-12-31
First posted
2025-10-03
Last updated
2025-10-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07206108. Inclusion in this directory is not an endorsement.