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Clinical Trials/NCT01532947
NCT01532947
Completed
Not Applicable

Survival of Endodontically Treated and Restored Premolars: A Randomized Controlled Trial

University of Siena0 sites360 target enrollmentJanuary 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Restoration Survival
Sponsor
University of Siena
Enrollment
360
Primary Endpoint
survival
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This in vivo study examined the contribution of remaining coronal dentin and placement of a prefabricated or customized fiber post to the six-year survival of endodontically treated premolars. A sample of 345 patients provided 6 groups of 60 premolars in need of endodontic treatment. Groups were classified according to the number of remaining coronal walls before abutment build-up. Within each group, teeth were allocated to three subgroups: A) no post-retention; B) LP; C) ES (N=20). All teeth were protected with a crown. Cox regression analysis was applied to assess whether the amount of residual coronal dentin and the type of endocanalar retention had a significant influence on failure risk of the restored teeth.

Registry
clinicaltrials.gov
Start Date
January 2003
End Date
June 2005
Last Updated
14 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Prof. Marco Ferrari

Professor

University of Siena

Eligibility Criteria

Inclusion Criteria

  • endodontically treated premolars with symptom-free root canal filling and a minimum apical seal of 4 mm, in occlusal function with a natural tooth and in interproximal contact with two adjacent natural teeth.

Exclusion Criteria

  • periapical lesion on the X-ray.

Outcomes

Primary Outcomes

survival

Time Frame: 2 years

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