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Dental Stem Cells and Bone Tissue Engineering (CELSORDINO)

C

Central Hospital, Nancy, France

Status

Unknown

Conditions

Tooth, Impacted

Treatments

Other: non-interventional study

Study type

Observational

Funder types

Other

Identifiers

NCT03194451
2017-A00860-53/EUDRACT

Details and patient eligibility

About

The main limitation in bone regeneration is the lack of vascularization of the newly shaped tissue. The main objective of this project is to check if the simultaneous differentiation of dental mesenchymal stem cells toward osteoblastic and endothelial lineage permits to obtain a new pre-vascularized tissue engineered bone construct.

We will then evaluate the boosting effect of the conditionned medium on cell differentiation and production of a prevascularized bone construct.

Full description

This project aims to develop a new pre-vascularized tissue engineered bone construct, using human cells of a simple and non invasive tissue source: dental pulp.

We will isolate mesenchymal stem cells from dental tissue of wisdom teeth, extracted from patients aged between 13 and 17 years old.

The objectives are: (i) to assess in combination the endothelial differentiation and osteoblastic differentiation of dental pulp stem cells (immature third molar); (ii) to study the boosting effect of the conditionned medium on cell differentiation and production of a prevascularized bone construct.

The differentiation will be monitored by evaluation of biosynthesized matrix, bone mineralization (immunohistochimie, Westen Blot), histological response (Von Kossa, Alizarin Red) and presence and quantification of pseudo-vascular structures (angiogenesis assay), compared to reference value (commercial differentiation medium).

Enrollment

40 estimated patients

Sex

All

Ages

13 to 17 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • patients aged between 13 and 17 years, who will come to Dental Service of University Regional Hospital Center of Nancy in order to have a tooth avulsion.
  • patient who has received a complete information about research organization and who is not opposed to the use of his own data.
  • patient who the representatives of parental authority have received a complete information about research organization and who are not opposed to the use of children's data.

Exclusion criteria

  • patients with local or general pathology

Trial contacts and locations

0

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Central trial contact

Vanessa MOBY, DD, PhD

Data sourced from clinicaltrials.gov

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