Recruiting

HeLP™

Sponsor:

Duke University

Code:

NCT07144228

Conditions

Prostate Cancer (Diagnosis)

Eligibility Criteria

Sex: Male

Age: 40+

Healthy Volunteers: Not accepted

Interventions

HeLP TM

Study Details

Brief summary:

This is a single center study evaluating whether a new blood test based on platelet proteins rather than plasma proteins can improve detection of prostate cancer and evaluate the degree of serious disease. Currently, doctors rely on multiple tests such as PSA, MRI scans and biopsies to do the same evaluation. Researchers are trying to see if HeLP™ can be a safe and accurate alternative.

The study is inviting men who are being seen for suspicion of prostate cancer (based on symptoms or previous lab results). If they agree to be in the study, the research team will take a sample of their blood at the time they are getting a repeat PSA test or having Imaging. The research test does not affect the care they are already receiving and takes 3 extra tubes of blood (\~3 tbsp).

The research team is aiming to include 300 participants total. They believe 278 people are needed to confidently compare results between people with and without prostate cancer.

They will do an interim analysis halfway through the study, once samples from 150 subjects have been collected.

The research is considered low risk-no more uncomfortable or dangerous than a blood draw. There is a risk of loss of privacy, but researchers are taking strong steps to protect privileged information. That includes proper data handling, secure, storage, and making sure the study team is trained in research ethics.

Conditions

Prostate Cancer (Diagnosis)

Study ID

NCT07144228

Start date

Mar 11, 2026

Status verified date

Aug, 2026

Completion date

Sep 30, 2028

Anticipated

Primary completion date

Sep 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 40+

Healthy Volunteers: Not accepted

Eligibility criteria

  • Patients ≥ 40 years of age
  • All patients with suspicion of PCa

Men ≥ 40 years of age attending Duke Health/Urology with suspicion of prostate cancer (Primary disease) will be approached to consent for the study. Upon consent, samples will be obtained alone, during repeat PSA/other biomarkers testing, or during imaging at Duke Lab.

Exclusion criteria

  • Men who have previously undergone treatment for prostate cancer.
  • Men with prior diagnosis of prostate cancer.
  • Men with severe, irreversible coagulopathy.
  • Men on anticoagulant therapies or those who have taken antiplatelet agents such as aspirin, NSAIDs (ibuprofen, entrophen, naproxen, diclofenac etc), clopidrogel, prasugrel, ticagrelor, or dipyridamole in the 7 days preceding blood collection.

Study Design

Enrollment

300 participants

Anticipated

Interventions and Outcome Measures

Arms

Control Group

Researchers are screening men who are suspicious of Pca, so those who will be negative for cancer will be the control group.

Case Group

Researchers are screening men who are suspicious of Pca, so those who will be diagnosed will be the case group.

Interventions

HeLP TM

lab test for prostate cancer

Primary outcome measure

  • Levels of HeLP™ proteins in the platelets of patients suspected to have PCa [ Time Frame: Baseline ]
  • Diagnostic accuracy as reported by area under the curve (AUC) [ Time Frame: Baseline ]

Central Contacts and Locations

Central contacts

Locations

Duke University

Recruiting

Durham, North Carolina, United States, 27710

Contacts

More Information

Sponsor

Duke University

Last update posted

Aug 6, 2026

Last verified

Aug, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Duke University on 2026-08-06.