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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01323894
Other study ID # ?DMR-99-IRB-122
Secondary ID
Status Completed
Phase N/A
First received March 24, 2011
Last updated June 15, 2016
Start date August 2011
Est. completion date July 2013

Study information

Verified date June 2016
Source China Medical University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

The first year purpose:

The best concentration of canonical Wnt3a will be investigated in promoting the osteoblastogenesis of human mesenchymal stem cells.


Description:

Our previous work is investigating the viral (Adv-BMP-2) administration for the development of a model to generate bones for possible use in clinical settings; the non-viral and viral administrations will be compared for best osteogenesis effects.

The first year purpose:

The best concentration of canonical Wnt3a will be investigated in promoting the osteoblastogenesis of human mesenchymal stem cells.


Recruitment information / eligibility

Status Completed
Enrollment 3
Est. completion date July 2013
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 80 Years
Eligibility Inclusion Criteria:

- age above 10 years old

- The patients require surgery ner iliac or abdomen areas

Exclusion Criteria:

- age below 10 years old

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan China Medical Universty Hospital Taichung

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Osteogenic Effects in Human Mesenchymal Stem Cells Enhanced by Wnt Signaling/Hydroxyapatite Nanoparticles--Comparisons between Non-viral and Viral administration in Tissue Engineered Bone Regeneration August 2011-July 2013 2 years No
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