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Positron Emission Tomography Using Carbon-11 Acetate in Finding Metastasis and Predicting Recurrence in Patients with Newly Diagnosed Prostate Cancer Who Are At Risk for Recurrence After Treatment - Article


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Carbon Monoxide Poisoning

Carbon Monoxide


Clinical Trial: Positron Emission Tomography Using Carbon-11 Acetate in Finding Metastasis and Predicting Recurrence in Patients with Newly Diagnosed Prostate Cancer Who Are At Risk for Recurrence After Treatment

This study is currently recruiting patients.

Sponsors and Collaborators: Barnes-Jewish Hospital
National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)

Purpose

RATIONALE: Diagnostic procedures, such as positron emission tomography using carbon-11 acetate, may help find metastasis from prostate cancer and may help predict whether prostate cancer will come back after treatment.

PURPOSE: This clinical trial is studying how well positron emission tomography using carbon-11 acetate works in finding metastasis and predicting recurrence in patients with prostate cancer who are at risk for recurrence after treatment.

Condition Intervention
stage I prostate cancer
stage II prostate cancer
stage III prostate cancer
stage IV prostate cancer
 Drug: carbon-11 acetate
 Procedure: diagnostic test
 Procedure: tomography, emission computed

MedlinePlus related topics:  Prostate Cancer

Study Type: Interventional
Study Design: Diagnostic

Official Title: Diagnostic Study of Positron Emission Tomography Using Carbon-11 Acetate in Detecting Metastasis and Predicting Recurrence in Patients with Newly Diagnosed Prostate Cancer At Medium Or High Risk for Recurrence After Initial Curative Therapy

Further Study Details: 

OBJECTIVES:

OUTLINE: Patients undergo positron emission tomography using carbon-11 acetate.

Patients are followed periodically.

PROJECTED ACCRUAL: A total of 285 patients will be accrued for this study.

Eligibility

Ages Eligible for Study:  18 Years   -   90 Years,  Genders Eligible for Study:  Both
Criteria

DISEASE CHARACTERISTICS:

PATIENT CHARACTERISTICS: Age

  • 18 to 90

Performance status

  • Not specified

Life expectancy

  • Not specified

Hematopoietic

  • Not specified

Hepatic

  • Not specified

Renal

  • Not specified

PRIOR CONCURRENT THERAPY: Biologic therapy

  • No prior or concurrent biologic therapy

Chemotherapy

  • No prior or concurrent chemotherapy

Endocrine therapy

Radiotherapy

  • No prior or concurrent radiotherapy

Surgery

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00121212


Missouri
      Siteman Cancer Center at Barnes-Jewish Hospital, Saint Louis,  Missouri,  63110,  United States; Recruiting
Tom R. Miller, MD, PhD  314-362-2809 

Study chairs or principal investigators

Tom R. Miller, MD, PhD,  Study Chair,  Barnes-Jewish Hospital   

More Information

Clinical trial summary from the National Cancer Institute''''s PDQ® database

Study ID Numbers:  CDR0000434994; WU-03-0315
Record last reviewed:  July 2005
Last Updated:  July 25, 2005
Record first received:  July 20, 2005
ClinicalTrials.gov Identifier:  NCT00121212
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-07-26


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October 13, 2008



Page Updated: December 17, 2004
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