A Feasibility Study to Determine PET/CT Imaging of Blood Flow to the Bone (PETCT)

University of California (UC) Davis

Status: Completed

Conditions: Normal Subjects

Treatments: Device: PET/CT Scan

Study type: Interventional

Funder types: Other

Identifiers

NCT03557450

1227928

Details and patient eligibility

About

To evaluate if a commonly used medical bone scan, called positron emission tomography/computed tomography (PET/CT) with sodium fluoride can measure bone blood flow to the hip.

Full description

The purpose of this research is to validate technique on a commonly used medical bone scan, called positron emission tomography/computed tomography (PET/CT) along with sodium fluoride as the tracer for determining blood flow to the bone. Up to 12 subjects will have PET/CT scans so that we can determine the repeatability and reliability of the images prior to using PET/CT for this use on subjects in the Phase 1b part of Dr. Nancy Lane's clinical research study entitled "A Phase 1, Randomized, Double-Blind, Placebo-Controlled Single and Multiple Ascending Dose Study of the Safety and Tolerability of Intravenous LLP2A-Alendronate in Adult Men and Women with Osteopenia Secondary to Glucocorticoids" (IRB Protocol #866350).

Enrollment: 3 patients

Sex: All

Ages: 20 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Subjects must meet all of the following criteria to be included in the study.

1. 20 - 75 years old

2. Must be ambulatory and able to attend all appointments

3. Women must agree to use one of the following methods of birth control for the duration of the clinical trial:

   systemic hormonal contraceptive (oral, injected, transdermal), intrauterine device, double barrier (e.g., cervical cap or diaphragm with condom or spermicide). Men with female partners must agree to use double barrier contraception, unless their partner is using systemic hormonal contraceptives or has an intrauterine device

4. Subject undergoing PET/CT scans must have the ability to lay motionless for up to 30 minutes.

Exclusion criteria

1. Subjects undergoing PET/CT scans must not be breast-feeding.
2. History of hypersensitivity to fluoride

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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3 participants in 1 patient group

PET/CT scanning with sodium fluoride

Experimental group

Description:

Subjects will received PET/CT scanning with sodium fluoride

Treatment:

Device: PET/CT Scan