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Clinical Trial Summary

This study aims to assess the hypothesis that revitalization of teeth without (a)symptomatic apical periodontitis have a more favourable outcome in terms of further root development, periapical bone healing, maintaining/regaining pulp sensitivity and survival, than teeth with (a)symptomatic apical periodontitis.


Clinical Trial Description

1. Trial objectives This study aims to investigate the effectiveness of revitalization procedures, in terms of maintaining or restoring periapical health, further root development and regaining of pulp sensitivity, in immature permanent teeth with (group 1) or without (group 2) (a)symptomatic apical periodontitis . 2. Primary endpoints RRA at 1 year post revitalization. 3 Secondary endpoints Maintained or restored periapical health (evaluated within each group separately due to expected baseline inequivalency between groups) 1 year post revitalization. 4 Other endpoints - RRA 2 and 3 years post revitalization - Maintained or restored periapical health 2 and 3 years post revitalization (evaluated within each group separately) - Pulp sensitivity 1-3 years post revitalization (evaluated within each group separately due to expected baseline inequivalency between groups) - Tooth survival 3 years post revitalization (even if no further root development and incomplete periapical bone healing with no clinical symptoms). 5 Trial Design Open, prospective cohort, multicenter Blinded: radiographic assessment and statistical analysis; operators and patients cannot be blinded, due to practically not feasible. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06043453
Study type Observational
Source Universitaire Ziekenhuizen KU Leuven
Contact Nastaran Meschi, MSc, PhD
Phone +32476313889
Email nastaran.meschi@ugent.be
Status Recruiting
Phase
Start date October 1, 2023
Completion date September 1, 2030

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