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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00670605
Other study ID # CDR0000584244
Secondary ID P30CA068485VU-VI
Status Terminated
Phase N/A
First received May 1, 2008
Last updated March 23, 2011
Start date June 2007

Study information

Verified date March 2011
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

RATIONALE: Gathering information about the number of young patients with cancer and the outcome of these patients may help doctors learn more about cancer.

PURPOSE: This research study is looking at the medical records of young patients undergoing cancer treatment at the Vanderbilt-Ingram Cancer Center to determine how often cancer occurs and the outcome of these patients.


Description:

OBJECTIVES:

- To determine the number of patients between 15 and 30 years old who are treated for newly diagnosed cancer at the Vanderbilt-Ingram Cancer Center (VICC), in middle Tennessee, and in the state of Tennessee between 1990 and 2005.

- To determine the outcomes of these patients.

- To determine the number of these patients enrolled on clinical trials at VICC.

- To compare the outcomes of these patients when treated on a trial versus not treated on a trial provided they have the same disease.

- To compare the number of these patients who are treated on a clinical trial when they are first seen at Vanderbilt Children's Hospital vs Vanderbilt University Hospital.

- To determine referral patterns of these patients to VICC.

- To compare the outcomes of these patients who are treated at VICC vs middle Tennessee vs the state of Tennessee vs the entire nation.

- To determine the reason for not enrolling on a clinical trial.

OUTLINE: Cancer cases taken from the Vanderbilt-Ingram Cancer Center (VICC) Registry and the Tennessee Cancer Registry are examined for number and types of cancer, mortality rates broken down by county and health department region, electronic medical records, and treatment outcomes. Data is analyzed for comparison of number of new cancer patients, mortality rates, and referral patterns at VICC versus number of new cancer patients in the region, state, and country.


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 30 Years
Eligibility DISEASE CHARACTERISTICS:

- Diagnosis of cancer

- Newly diagnosed disease from 1990 to 2005

- 15 to 30 years old at the time of cancer diagnosis

- Must live in the state of Tennessee

PATIENT CHARACTERISTICS:

- Not specified

PRIOR CONCURRENT THERAPY:

- Not specified

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Unspecified Adult Solid Tumor, Protocol Specific
  • Unspecified Childhood Solid Tumor, Protocol Specific

Intervention

Other:
medical chart review

study of socioeconomic and demographic variables


Locations

Country Name City State
United States Vanderbilt-Ingram Cancer Center Nashville Tennessee
United States Vanderbilt-Ingram Cancer Center - Cool Springs Nashville Tennessee
United States Vanderbilt-Ingram Cancer Center at Franklin Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with newly diagnosed cancer from 1990 to 2005 and treated at Vanderbilt-Ingram Cancer Center (VICC), in middle Tennessee, and the state of Tennessee No
Primary Comparison of outcomes No
Primary Number of patients enrolled in clinical trials at VICC No
Primary Outcomes of patients treated on a trial vs those not treated with the same disease No
Primary Comparison of number of patients treated at Vanderbilt Children's Hospital vs Vanderbilt University Hospital No
Primary Referral patterns No
Primary Reason for not enrolling on a clinical trial No
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