search
Back to results

Expression of Angiogenic Biomarkers During Healing of Intra-Oral Soft Tissue Engineered Grafts

Primary Purpose

Gingival Recession

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CelTx™
Free Gingival Graft
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gingival Recession focused on measuring gum, recession

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subject has signed informed consent to participate in Organogenesis Clinical Protocol 06-PER-002-CTX.
  • Subject has signed informed consent to participate in this adjunct bio-marker study.
  • Subject is willing to comply with the additional study visits at weeks 2 and 3 as required by this study.

Exclusion Criteria:

- Subject requires antibiotic prophylaxis for routine dental procedures.

Sites / Locations

  • Michigan Center for Oral Health Research

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CelTx™

Free Gingival Grafts

Arm Description

Living bilayered cell therapy product

Harvested tissue from palate

Outcomes

Primary Outcome Measures

Differences in Angiogenic Biomarkers
Within-subject difference between the concentrations at the CelTX and Free Gingival Graft areas
Differences in Angiogenic Biomarkers: PDGF-BB
Within-subject difference between the concentrations at the CelTX and Free Gingival Graft areas

Secondary Outcome Measures

Full Information

First Posted
May 20, 2010
Last Updated
July 19, 2017
Sponsor
University of Michigan
Collaborators
Organogenesis
search

1. Study Identification

Unique Protocol Identification Number
NCT01134081
Brief Title
Expression of Angiogenic Biomarkers During Healing of Intra-Oral Soft Tissue Engineered Grafts
Official Title
Expression of Angiogenic Biomarkers During Healing of Intra-Oral Soft Tissue Engineered Grafts
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
Organogenesis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this observational research study is to understand more about wound healing of gum tissue. This study was the biomarker study of a small cohort of study participants derived from NCT01547962 (completed). Two surgical sites of each patient were randomly selected to receive CelTx™ as a donor material in one site and conventional autograft using keratinized tissue from the palate as the donor material at the contralateral (opposite side) site. Fluids collected from between a tooth and the gum and directly from wounds contain proteins that occur in different levels as the wound healing process proceeds. In this research study wound fluid will be collected from the donor palate site (roof of your mouth) and the treated sites on your gum before and after placement of CelTx and conventional treatment (tissue from the roof of your mouth) to measure which proteins and how much of each are present during the first 4 weeks of wound healing.
Detailed Description
In a clinical trial designed to evaluate the safety and effectiveness of rhPDGF-BB to promote soft and hard tissue engineering of the periodontium, the subjects provided gingival crevicular fluid (GCF) or periodontal wound fluid (WF) and the results demonstrated contrasting inducible expression patterns of PDGF-AB, VEGF, and ICTP during periodontal healing [17, 24, 25]. However, little is known regarding the release of these molecules into local periodontal wound fluid during tissue-engineered grafts. The aim of this study is to determine the presence and influence of angiogenic biomarkers, such as PDGF, VEGF, and FGF, involved in the wound healing process of tissue engineered grafts in the treatment of subjects (with recession-type defects) who have an insufficient zone of attached gingival associated with at least two nonadjacent teeth. STUDY OBJECTIVES The purpose of this pilot study is to compare the expression of angiogenic biomarkers involved in the wound healing process of 2 different periodontal surgical approaches: 1) CelTx™ (living bilayered cell therapy product) and 2) free gingival grafts

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingival Recession
Keywords
gum, recession

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CelTx™
Arm Type
Experimental
Arm Description
Living bilayered cell therapy product
Arm Title
Free Gingival Grafts
Arm Type
Active Comparator
Arm Description
Harvested tissue from palate
Intervention Type
Biological
Intervention Name(s)
CelTx™
Intervention Description
CelTx™ is a living bilayered cell therapy product. CelTx™ is constructed of Type I bovine collagen (extracted from bovine tendons and subsequently purified) and viable allogeneic human fibroblasts and keratinocytes isolated from human neonatal foreskin. This is applied once in the oral cavity.
Intervention Type
Procedure
Intervention Name(s)
Free Gingival Graft
Intervention Description
Harvested tissue from palate
Primary Outcome Measure Information:
Title
Differences in Angiogenic Biomarkers
Description
Within-subject difference between the concentrations at the CelTX and Free Gingival Graft areas
Time Frame
5 time-points: pre-surgical, week(s) 1, 2, 3 and 4
Title
Differences in Angiogenic Biomarkers: PDGF-BB
Description
Within-subject difference between the concentrations at the CelTX and Free Gingival Graft areas
Time Frame
5 time-points: pre-surgical, week(s) 1, 2, 3 and 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject has signed informed consent to participate in Organogenesis Clinical Protocol 06-PER-002-CTX. Subject has signed informed consent to participate in this adjunct bio-marker study. Subject is willing to comply with the additional study visits at weeks 2 and 3 as required by this study. Exclusion Criteria: - Subject requires antibiotic prophylaxis for routine dental procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodrigo Neiva, DDS, MS
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michigan Center for Oral Health Research
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48106
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21248359
Citation
Morelli T, Neiva R, Nevins ML, McGuire MK, Scheyer ET, Oh TJ, Braun TM, Nor JE, Bates D, Giannobile WV. Angiogenic biomarkers and healing of living cellular constructs. J Dent Res. 2011 Apr;90(4):456-62. doi: 10.1177/0022034510389334. Epub 2011 Jan 19.
Results Reference
result

Learn more about this trial

Expression of Angiogenic Biomarkers During Healing of Intra-Oral Soft Tissue Engineered Grafts

We'll reach out to this number within 24 hrs