NCT02464202
Completed
Not Applicable
Use of Stereolithographic Model in Tooth Autotransplantation and Periodontal Ligament Stem Cells for Pulp Revascularization and Reinnervation to Increase the Success Rate for Tooth Replacement in Children
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Increase Success Rate of Tooth Transplantation
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- survival rate
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
The aim of this study lies in comparing the outcome of the proposed technique in a large sample size group to the outcome of the conventional tooth autotransplantation method and to provide sufficient evidence for improving the long-term success rate of the tooth autotransplantation procedure.
Investigators
Reinhilde Jacobs
Prof. Dr.
Universitaire Ziekenhuizen KU Leuven
Eligibility Criteria
Inclusion Criteria
- •The subjects will be divided in two groups according to different surgical protocols.
- •Pediatric subjects (age between 9-18 years) treated with the CBCT-based replica procedure (prospective approach).
- •Pediatric subjects (N=50) that missed their teeth due to agenesis or lost their permanent teeth due to trauma, caries, and endodontic failure and referred to dentistry department for replacement of the missing tooth by means of tooth autotransplantation.
- •Pediatric subjects (age between 9-18 years) treated with the conventional method (prospective and retrospective).
- •Pediatric subjects (N=50) that missed their teeth due to agenesis or lost their permanent teeth due to trauma, caries, and endodontic failure and referred to dentistry department for replacement of the missing tooth by means of tooth autotransplantation.
- •A matched control patient will be selected with the focus on a very similar surgical challenge, based on age, gender and a matching donor tooth with the same stage of root development and host bed.
Exclusion Criteria
- •Potential participants (case and control) will be excluded if follow-up data are missing for the one-year follow-up.
Outcomes
Primary Outcomes
survival rate
Time Frame: 5 years
success rate
Time Frame: 5 years
Study Sites (1)
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