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Clinical Trials/NCT00000111
NCT00000111
Unknown
Phase 1

Intraoral Grafting of Ex Vivo Produced Oral Mucosal Composites

National Center for Research Resources (NCRR)0 sitesJanuary 19, 2000
ConditionsMouth Diseases

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Mouth Diseases
Sponsor
National Center for Research Resources (NCRR)
Last Updated
20 years ago

Overview

Brief Summary

The purpose of this study is to see if we can develop a good graft for oral mucosal tissue that is like the top of the mouth in a "test tube" that could be used successfully in humans. We have already done this successfully mice. The next step is to take a small piece of tissue from a human volunteer and see if we can grow a larger piece of tissue from it outside the human body and graft it back into the same person successfully. We expect that this technique will work. It has already been tried in patients with burns of the skin who have had similar procedures where the skin is grafted back to them. The significance of this research is that oral tissue taken from the top of the mouth or palate is in limited supply and leaves the patient with a painful and uncomfortable post surgery experience. If we are successful with our technique the patient will experience less pain and discomfort from the site that we are using to grow our tissue outside the body than if we had taken it from the top of the mouth or palate. In addition, by waiting longer periods to grow the patient's cells we can make larger pieces of oral tissue than we could have gotten directly from the patient's mouth. Patients who will participate in this study will need to require a soft tissue graft from the mouth to an area that needs additional attached or keratinized mucosa. This will most likely be either in preparation for patients who have or will have dental implants placed. Another subset of patients are those who need scar tissue released or the vestibule of their mouth (area that turns from the gums to the lip) released.

Registry
clinicaltrials.gov
Start Date
January 19, 2000
End Date
TBD
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
National Center for Research Resources (NCRR)

Eligibility Criteria

Inclusion Criteria

  • Lack sufficient attached keratinized tissue at recipient surgical site in question

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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