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Skin and Blood Research Samples From Healthy Volunteers and Patients With Hematologic Diseases

Primary Purpose

Anemia, Sickle Cell

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Skin biopsy
Blood draw & sample
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Anemia, Sickle Cell focused on measuring Stem cells

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥ 18.
  • No active systemic skin infection at biopsy site.
  • No allergy to lidocaine or other local anesthetics

Exclusion Criteria:

ALL PATIENTS

  • History of a bleeding disorder, easy bleeding, or bruising.
  • Inability or unwillingness to provide informed consent.

SICKLE CELL PATIENTS

  • Platelets ≤ 50,000
  • INR ≥ 1.5
  • Currently bing given intravenous heparin

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Healthy Volunteers

Patients with benign, inherited hematologic disease

Arm Description

To obtain a one time skin sample (4 ml skin punch biopsy) and one time blood sample (1 teaspoon)

To obtain a one time skin sample (4 ml skin punch biopsy) and one time blood sample (1 teaspoon)

Outcomes

Primary Outcome Measures

Obtain skin biopsy samples from normal healthy volunteers and patients with a benign, inherited hematologic disease to created induced pluripotent stem cells
Only one biopsy but analysis may take one year.

Secondary Outcome Measures

Define the efficiency of homologous recombination in induced pluripotent stem cells derived from skin biopsy samples.
Only one blood draw and biopsy but analysis may take one year.
Define the efficiency of homologous recombination in human embryonic stem cells using NIH-approved cell lines
Only one blood draw and biopsy but analysis may take one year.
Establish the genetic consequences of the derivation of human induced pluripotent cells in normal controls or patients with benign, inherited hematologic diseases, by genomic analysis, including whole genome sequencing
Only one blood draw and biopsy but analysis may take one year.
Obtain blood samples to confirm genetic mutations in patients with an inherited hematologic disease
Only one blood draw but analysis may take one year.

Full Information

First Posted
February 9, 2009
Last Updated
July 9, 2013
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00840567
Brief Title
Skin and Blood Research Samples From Healthy Volunteers and Patients With Hematologic Diseases
Official Title
Acquisition of Skin Biopsies and Blood Samples From Normal Volunteers and Patients With Benign, Inherited Hematologic Diseases for Research Purposes
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Terminated
Why Stopped
Key samples protocols will be provided by a collaborator and we were not able to produce IPS lines from human fibroblasts.
Study Start Date
February 2009 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators plan to obtain skin and blood samples from healthy volunteers and patients with a benign, inherited hematologic disease to use for research to use homologous recombination to correct β-globin gene mutations in therapeutically useful cells, like autologous induced pluripotent stem cells from sickle cell anemia patients.
Detailed Description
To obtain skin biopsy samples from normal healthy volunteers and patients with a benign, inherited hematologic disease, such as sickle cell anemia, to create induced pluripotent stem cells. Pluripotency will be confirmed by injecting potential iPS cell lines into immunodeficient mice, assessing the ability of each line to cause cystic teratomas in recipient mice. To define the efficiency of homologous recombination in induced pluripotent stem cells derived from skin biopsy samples. To define the efficiency of homologous recombination in human embryonic stem cells using NIH-approved cell lines. To establish the genetic consequences of the derivation of human induced pluripotent cells in normal controls or patients with benign, inherited, hematologic diseases, by genomic analysis, including whole genome sequencing. To establish the genetic consequences of homologous recombination in human induced pluripotent stem cells and embryonic stem cells by genomic analysis, including whole genome sequencing. To obtain blood samples to confirm genetic mutations in patients with an inherited hematologic disease (and to confirm no mutations in healthy volunteers).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Sickle Cell
Keywords
Stem cells

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy Volunteers
Arm Type
Other
Arm Description
To obtain a one time skin sample (4 ml skin punch biopsy) and one time blood sample (1 teaspoon)
Arm Title
Patients with benign, inherited hematologic disease
Arm Type
Other
Arm Description
To obtain a one time skin sample (4 ml skin punch biopsy) and one time blood sample (1 teaspoon)
Intervention Type
Procedure
Intervention Name(s)
Skin biopsy
Intervention Type
Procedure
Intervention Name(s)
Blood draw & sample
Primary Outcome Measure Information:
Title
Obtain skin biopsy samples from normal healthy volunteers and patients with a benign, inherited hematologic disease to created induced pluripotent stem cells
Description
Only one biopsy but analysis may take one year.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Define the efficiency of homologous recombination in induced pluripotent stem cells derived from skin biopsy samples.
Description
Only one blood draw and biopsy but analysis may take one year.
Time Frame
1 year
Title
Define the efficiency of homologous recombination in human embryonic stem cells using NIH-approved cell lines
Description
Only one blood draw and biopsy but analysis may take one year.
Time Frame
1 year
Title
Establish the genetic consequences of the derivation of human induced pluripotent cells in normal controls or patients with benign, inherited hematologic diseases, by genomic analysis, including whole genome sequencing
Description
Only one blood draw and biopsy but analysis may take one year.
Time Frame
1 year
Title
Obtain blood samples to confirm genetic mutations in patients with an inherited hematologic disease
Description
Only one blood draw but analysis may take one year.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 18. No active systemic skin infection at biopsy site. No allergy to lidocaine or other local anesthetics Exclusion Criteria: ALL PATIENTS History of a bleeding disorder, easy bleeding, or bruising. Inability or unwillingness to provide informed consent. SICKLE CELL PATIENTS Platelets ≤ 50,000 INR ≥ 1.5 Currently bing given intravenous heparin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy Ley, M.D.
Organizational Affiliation
Washington Univerisity School of Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
Washington University School of Medicine
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
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18157115
Citation
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Citation
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Links:
URL
http://www.siteman.wustl.edu
Description
Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

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Skin and Blood Research Samples From Healthy Volunteers and Patients With Hematologic Diseases

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