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Thyroid Cancer Collaborative Registry of Patients With Thyroid Cancer and/or Thyroid Nodules
This study is currently recruiting participants.
Verified by National Cancer Institute (NCI), December 2008
Sponsors and Collaborators: University of Nebraska
National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00693368
  Purpose

RATIONALE: Gathering information about patients with thyroid cancer or thyroid nodules may help the study of thyroid cancer in the future.

PURPOSE: This study is gathering information and tissue and blood samples from patients with thyroid cancer or thyroid nodules.


Condition Intervention
Head and Neck Cancer
Procedure: biologic sample preservation procedure
Procedure: medical chart review
Procedure: psychosocial assessment and care
Procedure: quality-of-life assessment
Procedure: questionnaire administration
Procedure: study of high risk factors
Procedure: study of socioeconomic and demographic variables
Procedure: survey administration

MedlinePlus related topics: Cancer Head and Neck Cancer Thyroid Cancer
Drug Information available for: Thyroid
U.S. FDA Resources
Study Type: Observational
Official Title: Development and Implementation of The Thyroid Cancer Collaborative Registry (TCCR)

Further study details as provided by National Cancer Institute (NCI):

Primary Outcome Measures:
  • Development and implementation of a web-based Thyroid Cancer Collaborative Registry at the University of Nebraska Medical Center (UNMC)/Nebraska Medical Center (NMC) [ Designated as safety issue: No ]
  • Standardization of clinical, environmental, socio-demographic, and family history data for thyroid cancer research [ Designated as safety issue: No ]
  • Procurement and banking of excess biological material (i.e., thyroid tissue, tumor tissue and/or metastatic thyroid cancer tissue and/or paraffin embedded tissue) for future analysis [ Designated as safety issue: No ]
  • Collection and banking of blood and serum samples for future analysis that will be proposed in future IRB submissions [ Designated as safety issue: No ]
  • Establishment of a high-risk cohort for future research into the molecular and biological bases of thyroid cancer susceptibility and for interventional trials [ Designated as safety issue: No ]

Estimated Enrollment: 2000
Study Start Date: February 2008
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   19 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

DISEASE CHARACTERISTICS:

  • Meets either of the following criteria:

    • Current diagnosis or history of thyroid cancer
    • Presence of one or more thyroid nodules

PATIENT CHARACTERISTICS:

  • Able to provide informed consent

PRIOR CONCURRENT THERAPY:

  • Not specified
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00693368

Locations
United States, Nebraska
UNMC Eppley Cancer Center at the University of Nebraska Medical Center Recruiting
Omaha, Nebraska, United States, 68198-6805
Contact: Clinical Trials Office - UNMC Eppley Cancer Center at the Univ     800-999-5465        
Sponsors and Collaborators
University of Nebraska
Investigators
Principal Investigator: Whitney S. Goldner, MD University of Nebraska
  More Information

Clinical trial summary from the National Cancer Institute's PDQ® database  This link exits the ClinicalTrials.gov site

Study ID Numbers: CDR0000588891, UNMC-46307
Study First Received: June 6, 2008
Last Updated: December 31, 2008
ClinicalTrials.gov Identifier: NCT00693368  
Health Authority: Unspecified

Keywords provided by National Cancer Institute (NCI):
thyroid cancer

Study placed in the following topic categories:
Thyroid Nodule
Thyroid Neoplasms
Head and Neck Neoplasms
Endocrine System Diseases
Endocrinopathy
Thyroid Diseases
Endocrine Gland Neoplasms

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Site

ClinicalTrials.gov processed this record on January 16, 2009