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Clinical Trials/NCT03485794
NCT03485794
Terminated
N/A

Metabolic Profiling of Peripheral Blood Mononuclear Cells (PBMCs) by LC-MS in Prostate Cancer Patients

University of Southern California1 site in 1 country10 target enrollmentNovember 14, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Carcinoma
Sponsor
University of Southern California
Enrollment
10
Locations
1
Primary Endpoint
Blood sample collection
Status
Terminated
Last Updated
8 months ago

Overview

Brief Summary

This pilot research trial utilizes the collection of blood in studying metabolites in patients with prostate cancer. Metabolites are the small molecule products of cellular metabolism that are produced naturally in all living cells. Collecting blood in order to study metabolites may help doctors monitor and treat prostate cancer more effectively.

Detailed Description

PRIMARY OBJECTIVES: I. Develop blood sample collection and preparation procedures for reliable, meaningful metabolomic profiling of peripheral blood mononuclear cells (PBMCs) by liquid chromatography/quadruple-time of flight/mass spectrometry (LC/Q-TOF/MS) that can be implemented in a clinical setting. II. Optimize data analysis methods and software usage to create a metabolic profile for patients at the time of blood collection. III. Compare metabolite profiles of isolated PBMCs versus (vs.) other blood fractions (plasma, red blood cells \[RBCs\], and whole blood). IV. Identify elements of the PBMC metabolite profile that may correlate to patient disease state. OUTLINE: Patients undergo collection of blood for metabolic profiling via LC/Q-TOF/MS.

Registry
clinicaltrials.gov
Start Date
November 14, 2017
End Date
January 2, 2024
Last Updated
8 months ago
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All subjects will have histologically confirmed prostate cancer
  • Provide written consent/authorization to participate in this study
  • Have no signs or symptoms of active infection
  • Exhibit a willingness to comply with the experimental procedures as outlined in this protocol

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Blood sample collection

Time Frame: Baseline

The blood will be used to analyze the metabolites produced by white blood cells.

Study Sites (1)

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