Development of Bone Grafts Using Adipose Derived Stem Cells and Different Scaffolds
This study is currently recruiting participants.
Verified February 2012 by University of Zurich
Sponsor:
University of Zurich
Information provided by (Responsible Party):
University of Zurich
ClinicalTrials.gov Identifier:
NCT01218945
First received: September 29, 2010
Last updated: February 23, 2012
Last verified: February 2012
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Purpose
The repair of large osseous defects remains still unsolved. Aim of this study is to isolate and cultivate fat-derived progenitor cells and differentiation into osteoblasts. Therefore, our research idea is to pre-engineer large synthetic bone grafts and study the vascularization process in vivo.
| Condition | Intervention |
|---|---|
|
Overweight |
Procedure: Cell Culture |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Development of Bone Grafts Using Adipose Derived Stem Cells and Different Scaffolds: Impact of Pre-engineered Capillaries in Critical Size Grafts |
Resource links provided by NLM:
Further study details as provided by University of Zurich:
Biospecimen Retention: Samples With DNA
Human adipose-derived stem cells from human fat
| Estimated Enrollment: | 100 |
| Study Start Date: | November 2009 |
| Estimated Study Completion Date: | August 2012 |
| Estimated Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Fat Removal
Patients undergoing surgical fat removal
|
Procedure: Cell Culture
Aim of this study is to isolate and cultivate fat-derived progenitor cells and differentiation into osteoblasts. Therefore, our research idea is to pre-engineer large synthetic bone grafts and study the vascularization process in vivo.
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients admitted for reconstructive surgery
Criteria
Inclusion criteria:
- German-speaking patients aged 18-70 admitted to the Clinic of Reconstructive surgery for reconstructive surgery and fat-excision.
Exclusion criteria:
- Drug-abuse, neoplasia and metabolic disorders
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01218945
Contacts
| Contact: Maurizio Calcagni, MD | +41 (0)44 255 11 11 | maurizio.calcagni@usz.ch |
Locations
| Switzerland | |
| University Hospital Zurich, Clinic of Reconstructive Surgery | Recruiting |
| Zurich, ZH, Switzerland, 8091 | |
| Contact: Maurizio Calcagni maurizio.calcagni@usz.ch | |
| Contact: Guido Wanner guido.wanner@usz.ch | |
Sponsors and Collaborators
University of Zurich
Investigators
| Principal Investigator: | 01 Studienregister MasterAdmins, MD | University Hospital Zurich, Clinic of Reconstructive Surgery |
More Information
No publications provided
| Responsible Party: | University of Zurich |
| ClinicalTrials.gov Identifier: | NCT01218945 History of Changes |
| Other Study ID Numbers: | Bone-ZH09 |
| Study First Received: | September 29, 2010 |
| Last Updated: | February 23, 2012 |
| Health Authority: | Switzerland: Swissmedic |
Additional relevant MeSH terms:
|
Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 22, 2013