Analysis of Cutaneous and Hematologic Disorders by High-Throughput Nucleic Acid Sequencing

This study is currently recruiting participants.
Verified April 2013 by Stanford University
Sponsor:
Information provided by (Responsible Party):
Stanford University
ClinicalTrials.gov Identifier:
NCT01556828
First received: March 14, 2012
Last updated: April 16, 2013
Last verified: April 2013

March 14, 2012
April 16, 2013
June 2011
April 2014   (final data collection date for primary outcome measure)
Number of mutations [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Identify mutations, changes in DNA copy number, structural rearrangements, or altered coding and non-coding RNA expression
Same as current
Complete list of historical versions of study NCT01556828 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Analysis of Cutaneous and Hematologic Disorders by High-Throughput Nucleic Acid Sequencing
Analysis of Cutaneous and Hematologic Disorders by High-Throughput Nucleic Acid Sequencing

The goal of this study is to identify genetic changes associated with the initiation, progression, and treatment response of response of cutaneous and hematologic disorders using recently developed high-throughput sequencing technologies. The improved understanding of the genetic changes associated with cutaneous and hematologic disorders may lead to improved diagnostic, prognostic and therapeutic options for these disorders.

Not Provided
Observational
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:

whole blood tissue

Non-Probability Sample

Eligible subjects will be identified and recruited by referral from that individual's treating physician, mainly Stanford-affiliated dermatologists, oncologists, and hematologists.

  • Cutaneous Lymphoma
  • Other Skin Disorders
  • Mycosis Fungoides
  • Cutaneous T-cell Lymphoma
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Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
30
April 2015
April 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18 years of age or older
  • Patient meets the clinical and/or pathologic criteria for the cutaneous or hematologic disorder being examined.
  • Patient is willing to provide skin biopsies and five 10 mL tubes of peripheral blood.

Exclusion Criteria:

- Less than 18 years of age

Both
18 Years and older
No
Contact: Alexander Ungewickell 650-723-6661 ungewica@stanford.edu
United States
 
NCT01556828
LYMNHL0091, SU-03142012-9329, 21750
Yes
Stanford University
Stanford University
Not Provided
Principal Investigator: Paul Khavari, MD Stanford University
Stanford University
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP