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Clinical Trials/NCT00580203
NCT00580203
Completed
Not Applicable

Collection of Tissue, Blood, and Other Specimens From Patients With Head and Neck Diseases to Study the Causes, Diagnosis, Prevention and Treatment of Cancers

Memorial Sloan Kettering Cancer Center1 site in 1 country1,468 target enrollmentFebruary 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Head and Neck Cancers
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
1468
Locations
1
Primary Endpoint
Collect tissues, blood, and other specimens from patients with malignant or nonmalignant diseases of the head and neck. Specimens will be used to investigate growth, development, and transformation of normal and abnormal cells in the future.
Status
Completed
Last Updated
last year

Overview

Brief Summary

This is a protocol to collect tissues, blood, and other specimens from patients with malignant or nonmalignant diseases of the head and neck. Collected specimens will be used in laboratory studies to investigate the growth, development, and transformation of normal and abnormal cells in the future.

Detailed Description

This is a protocol to collect tissues, blood, and other specimens from patients with malignant or nonmalignant diseases of the head and neck. Collected specimens will be used in laboratory studies to investigate the growth, development, and transformation of normal and abnormal cells in the future.

Registry
clinicaltrials.gov
Start Date
February 2004
End Date
November 12, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with head and neck diseases are eligible if they have had tissue, serum, urine, or other specimens removed or collected for diagnostic or therapeutic purposes.
  • Patients will be entered onto this protocol without preference for any racial or ethnic group.
  • Patients may have received prior chemotherapy, radiation, surgical therapy, immunotherapy, or differentiation therapy.
  • The specimen collected must be large enough to allow conventional testing necessary for patient care, with the portion of the specimen reserved for research laboratory analysis excised from residual tissue that would otherwise have been discarded.

Exclusion Criteria

  • Patients not giving informed consent will be excluded.

Outcomes

Primary Outcomes

Collect tissues, blood, and other specimens from patients with malignant or nonmalignant diseases of the head and neck. Specimens will be used to investigate growth, development, and transformation of normal and abnormal cells in the future.

Time Frame: 36 months

Study Sites (1)

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