Sodium Fluoride PET/CT for the Evaluation of Skeletal Cancer

NCT ID: NCT01541358

Last Updated: 2017-06-14

Study Results

Results available

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Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-05-31

Study Completion Date

2012-09-30

Brief Summary

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This clinical trial studies fluorine F-18 sodium fluoride positron emission tomography (PET)/computed tomography (CT) in diagnosing bone tumors in patients with cancer. Diagnostic procedures, such as fluorine F-18 sodium fluoride PET/CT, may help find and diagnose bone cancer

Detailed Description

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The objective of the study is to use 18F sodium fluoride (fluorine F-18 sodium fluoride) PET/CT scanning to detect and characterize lesions in patients who have suspected skeletal malignancy. We hypothesize that scanning with 18F-NaF (fluorine F-18 sodium fluoride) is more sensitive for skeletal abnormalities and may better characterize lesions than conventional imaging.

Conditions

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Bone Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Diagnostic (fluorine F 18 sodium fluoride PET/CT)

Patients undergo fluorine F 18 sodium fluoride PET/CT scan.

Group Type EXPERIMENTAL

fluorine F 18 sodium fluoride

Intervention Type RADIATION

Undergo fluorine F 18 sodium fluoride PET/CT scan

positron emission tomography/computed tomography

Intervention Type PROCEDURE

Undergo fluorine F 18 sodium fluoride PET/CT scan

Interventions

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fluorine F 18 sodium fluoride

Undergo fluorine F 18 sodium fluoride PET/CT scan

Intervention Type RADIATION

positron emission tomography/computed tomography

Undergo fluorine F 18 sodium fluoride PET/CT scan

Intervention Type PROCEDURE

Other Intervention Names

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18 F-NaF F-18 NaF

Eligibility Criteria

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Inclusion Criteria

* Patients referred for evaluation of suspected skeletal cancer
* Patients must understand and voluntarily sign an informed consent form after the contents have been fully explained to them

Exclusion Criteria

* Patients who cannot complete a PET/CT scan
* Pregnant women
* Healthy volunteers
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Andrew Quon

Associate Professor of Radiology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Andrew Quon

Role: PRINCIPAL_INVESTIGATOR

Stanford University

Locations

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Stanford University

Stanford, California, United States

Site Status

Countries

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United States

Other Identifiers

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NCI-2012-00138

Identifier Type: REGISTRY

Identifier Source: secondary_id

SU-02162012-9128

Identifier Type: OTHER

Identifier Source: secondary_id

VAR0074

Identifier Type: OTHER

Identifier Source: secondary_id

IRB-23082

Identifier Type: -

Identifier Source: org_study_id

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