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Clinical Trials/NCT01548261
NCT01548261
Unknown
Not Applicable

Donating Oral Mucosal Cells for the Study of ex Vivo Culture of Cells Sheets

National Taiwan University Hospital1 site in 1 country1 target enrollmentJanuary 2012
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
National Taiwan University Hospital
Enrollment
1
Locations
1
Last Updated
14 years ago

Overview

Brief Summary

Cultivated oral mucosal epithelial sheets on amniotic membrane have been reported to have good clinical results in treating patients with ocular surface disorders in both human and animal studies. However, such technique has not been well established in this hospital. The main purpose of this study is to obtain the discarded oral mucosal tissue from healthy donors who volunteer to donate their oral mucosa from buccal area. The obtained oral mucosal tissue will be cultured under different types (co-culture with or without 3T3 cells)。Inverted light microscopy, electron microscopy and immunostaining with K3/K12, K14, Ki67, P63, connexin 43, and involucrin will be preformed to test the effects of foreskin cell line co-culture system on cell condition. The investigators plan to start the study from Jan. 1st, 2011 to Dec. 31th, 2015. Thirty patients will be enrolled.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
December 2015
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

National Taiwan University Hospital

Wei-Li Chen/Assistant Professor, National Taiwan University, Department of Ophthalmology.

National Taiwan University Hospital

Eligibility Criteria

Inclusion Criteria

  • The age 20 to 55 year-old healthy contributor.
  • does not have disease of the oral cavity.

Exclusion Criteria

  • In the past had the oral mucosa disease, wound cicatrization bad, or hemoglutination condition not good medical history. Sickness must stop using above any anti-hemoglutination medicine one week.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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