ClinicalTrials.Veeva

Menu

Collection of Blood in Studying Metabolites in Patients With Prostate Cancer

University of Southern California logo

University of Southern California

Status

Enrolling

Conditions

Prostate Carcinoma

Treatments

Other: Laboratory Biomarker Analysis
Procedure: Biospecimen Collection

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT03485794
NCI-2017-02078 (Registry Identifier)
4P-17-8 (Other Identifier)
P30CA014089 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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.

Enrollment

10 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial design

10 participants in 1 patient group

Diagnostic (biospecimen collection)
Description:
Patients undergo collection of blood for metabolic profiling via LC/Q-TOF/MS.
Treatment:
Other: Laboratory Biomarker Analysis
Procedure: Biospecimen Collection

Trial contacts and locations

1

Loading...

Central trial contact

Brandi Scott

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems