Using Serum Parathyroid Hormones and Calcium to Improve Prostate Cancer Diagnosis

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Completed
CT.gov ID
NCT02397629
Collaborator
(none)
62
1
36
1.7

Study Details

Study Description

Brief Summary

This is a cross sectional study to examine the relationship between serum calcium and PTHrP and serum PSA in men referred for prostate biopsy at Wake Forest University.

Condition or Disease Intervention/Treatment Phase
  • Other: This study has no intervention

Detailed Description

This is a cross sectional study to examine the relationship between serum calcium and PTHrP and serum PSA in men referred for prostate biopsy at Wake Forest University. Men scheduled for biopsy will be approached by the study nurse who will explain the study and invite the men to participate. After the patients provide written consent, she/he will obtain the following information from the patient chart: age, race (self-report, white, black, other), height, weight (for determination of Body Mass Index, a variable reported to influence PSA). Blood draw for study analytes will be coordinated with routine blood draw for PSA testing to minimize the need for an additional needle stick. A copy of the informed consent is given to the patient and the original is placed in a file for the P.I.

The biopsy status of men at the time they are invited to participate is unknown. Men are "sorted" into cancer and non-cancer groups only after their biopsies are read. Serum samples are sent to the Department of Laboratory Medicine at Wake Forest. All assays are performed "in house". Based on consultation with our urologists, we anticipate that approximately 30% of the biopsies will be positive (i.e., prostate cancer). The majority (approximately 70%) will be negative (benign). Approximately 1-2% of the biopsies may be classified as "indeterminate". Because there will not be a sufficient number of "indeterminate" pathologies to be treated as a separate category, this group will not be analyzed further. However, men with "indeterminate" biopsies are eligible for the study if they are re-biopsied.

Study Design

Study Type:
Observational
Actual Enrollment :
62 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Using Serum Parathyroid Hormones and Calcium to Improve Prostate Cancer Diagnosis
Study Start Date :
May 1, 2013
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
May 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Patients Undergoing Prostate Biopsy

Men referred for biopsy because of an abnormal or suspicious PSA digital rectal exam, or both.

Other: This study has no intervention

Outcome Measures

Primary Outcome Measures

  1. To measure the relationship of calcium and PTH levels to PSA levels in patients receiving a prostate biopsy. [Day 1]

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Men age > 40 years

  • Men referred for biopsy because of an abnormal or suspicious PSA digital rectal exam, or both.

  • Ability and willingness to sign a written, IRB-approved informed consent document

Exclusion Criteria:
  • Men using drugs known to interfere with serum PSA or with serum PTHrP and calcium. Drugs known to interfere with PSA include 5-alpha-reductase inhibitors (Proscar). Drugs known to interfere with calcium and/or PTH include lithium and thiazide diuretics.

  • Patients with prior transurethral resection of the prostate (TURP) or equivalent procedure (laser incision). In these men the reduction in prostatic volume may give a biased estimate of the relationship between PSA, calcium and PTHrP.

  • Patients on dialysis. These are excluded because dialysis increases the percentage of free PSA in serum.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Comprehensive Cancer Center of Wake Forset University Winston-Salem North Carolina United States 27157

Sponsors and Collaborators

  • Wake Forest University Health Sciences

Investigators

  • Principal Investigator: Ram Pathak, MD, Wake Forest University Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wake Forest University Health Sciences
ClinicalTrials.gov Identifier:
NCT02397629
Other Study ID Numbers:
  • IRB00014769
  • CCCWFU 85B10
First Posted:
Mar 25, 2015
Last Update Posted:
Mar 11, 2022
Last Verified:
Jul 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2022