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Status unknownNCT03194451CELSORDINOUpdated Jun 23, 2017

Dental Stem Cells and Bone Tissue Engineering (CELSORDINO)

An observational study in Tooth, Impacted, sponsored by Central Hospital, Nancy, France. Status unknown. Open to participants aged 13 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-06-23.

Sponsored by Central Hospital, Nancy, France · Observational

The sponsor has not verified this record recently (last verified Jun 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
40
Ages
13 Years to 17 Years
Sex
All
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Study summary

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.

Read the detailed 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).

02

Conditions studied

  • Tooth, Impacted

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Keywords

  • bone tissue engineering, dental stem cell differentiation
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In context

Tooth, Impacted

200 studies on the registry are indexed under Tooth, Impacted; 21 are open to participants now.

This study's planned enrollment of 40 is below the median of 60 across 31 observational studies indexed under Tooth, Impacted.

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Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 796 studies on the registry; 187 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients aged between 13 and 17 years, who will be operated for wisdom tooth avulsion

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • patients with local or general pathology
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Interventions

  • Othernon-interventional study

    teeth collection

06

What researchers measure

Primary outcomes

  1. Bone mineralization

    Measured parameter is equal or superior to reference value (commercial differentiation medium)

    Time frame: Day 28 of cell culture

Secondary outcomes

  1. presence and quantification of pseudo-vascular structures

    Measured parameter is equal or superior to reference value (commercial differentiation medium)

    Time frame: Day 28 of cell culture

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 23, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03194451
Responsible party
Sponsor
First posted
Jun 21, 2017
Start date
Jul 10, 2017 (estimated)
Primary completion
Aug 20, 2017 (estimated)
Completion
Jul 10, 2019 (estimated)
Last update
Jun 23, 2017

Study contacts

Vanessa MOBY, DD, PhD
Contact
vanessa.moby@univ-lorraine.fr
0383154256 ext. 33
Vanessa MOBY, DD, PhD
principal investigator · IMoPA, UMR-CNRS 7365 CNRS-UL, Medicine Faculty

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2017. You cannot join it, but the record below documents what was studied.

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