Actively Recruiting

Phase Not Applicable
Age: 18Years +
MALE
NCT04581109

Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer (EPIDROP)

Led by University Hospital, Montpellier · Updated on 2025-07-10

100

Participants Needed

2

Research Sites

226 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The use of liquid biopsy could be the key for precision medicine. Circulating tumor cells (CTCs) are the most studied circulating biomarkers used to assess the metastatic process and they have shown their clinical validity and utility in cancer patients. However, their detection and capture are still a challenge as they are very rare in the bloodstream. In this clinical trial named "EPIDROP", the investigators will use an innovative device called EPIDROP (for EPIspot in a DROP) in metastatic prostate cancer. EPIDROP is a completely new technology answering to biological and clinical questions by proposing a procedure detecting the functional subset of prostatic CTCs at the single cell level. The investigators will stain cells in the sample for EpCAM, PSMA, CD45 before to encapsulate them one by one in microdroplets and measure the PSA secretion by only the viable CTCs. This study aims to demonstrate the non-inferiority of the EPIDROP compared to the CellSearch system.

CONDITIONS

Official Title

Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer (EPIDROP)

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Be male and at least 18 years old
  • Have metastatic prostate cancer that is either untreated or in biological or clinical recurrence after hormone suppression (mCRPC)
Not Eligible

You will not qualify if you...

  • Have non-metastatic prostate cancer in biological or clinical recurrence after hormone suppression (nmCRPC)
  • Have had another active or treated cancer within the last 5 years
  • Be under legal protection such as guardianship or curatorship
  • Be deprived of liberty by administrative decision
  • Not be affiliated with or a beneficiary of a social security plan
  • Be currently excluded from participation in another clinical trial
  • Be unable to understand or respond to questionnaires
  • Be unable to understand the nature, purpose, and methods of the study
  • Refuse to sign informed consent

AI-Screening

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Trial Site Locations

Total: 2 locations

1

University Hospital Center

Montpellier, Occitanie, France, 34295

Active, Not Recruiting

2

University Center, Hospital

Nîmes, France

Actively Recruiting

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Research Team

C

Catherine ALIX-PANABIERES, MCU-PH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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