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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02740907
Other study ID # Premolar transplantation
Secondary ID
Status Completed
Phase N/A
First received March 22, 2016
Last updated April 12, 2016
Start date August 2012
Est. completion date October 2014

Study information

Verified date April 2016
Source MKG-Praxisklinik
Contact n/a
Is FDA regulated No
Health authority Germany: Ministry of Health
Study type Observational

Clinical Trial Summary

Objective:

Premolar autotransplantation represents an effective therapeutic option for the treatment of juvenile dentition in traumatic dental injury with tooth loss. Numerous studies report on the osteoinductive potency of the method, however, to date no quantitative data has been provided. The objective of this prospective clinical study was to quantitatively assess the bone and soft tissue levels after autogenous premolar transplantation by clinical and radiographic parameters.

Materials/Methods:

In the study 26 premolars were transplanted in 20 patients after traumatic dental injury (n=10) or tooth aplasia (n=16) in the upper front. Standard clinical parameters were evaluated. Based on a standardized photo documentation, the relative soft tissue level was measured in comparison to the healthy adjacent teeth. Radiographic findings involved the evaluation of root resorption, pulp canal obliterations and the relative bone height. Patient satisfaction was determined using a standardized questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 17 Years
Eligibility Inclusion Criteria:

- premolar transplantation after tooth loss in the anterior maxilla (13-23) by aplasia or trauma

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Procedure:
premolar autotransplantation
Autogenous tooth transplantation of premolars to the anterior maxilla to stimulate bone and soft tissue growth.

Locations

Country Name City State
Germany MKG Praxisklinik Munich Sauerbruchstraße 48

Sponsors (1)

Lead Sponsor Collaborator
MKG-Praxisklinik

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Transplant survival Evaluation by Kaplan-Meier-Estimator. 2006-2014 No
Primary Soft tissue development Measurement by standardized clinical documentation. 2006-2014 No
Primary Bone development Measurement by radiographic evaluation. 2006-2014 No
Primary Sensibility Assessment of clinical sensibility. 2006-2014 No
Primary Root resorptions Radiographic evaluation. 2006-2014 No
Primary Pulp obliteration Radiographic evaluation. 2006-2014 No
See also
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