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EPISPOT Detection of Circulating Prostate Cells Among Adenocarcinoma Patients

C

Centre Hospitalier Universitaire de Nīmes

Status

Unknown

Conditions

Adenocarcinoma of the Prostate

Treatments

Biological: CellSearch detection of the number of circulating, functional, prostate cells
Biological: EPISPOT detection of the number of circulating cells

Study type

Observational

Funder types

Other

Identifiers

NCT01402154
2011-A00328-33 (Other Identifier)
AOI/2010/SD-01

Details and patient eligibility

About

The primary objective of this study is to evaluate the predictive value (in terms of remission) of a new technique for detecting circulating, functional, prostate cells among patients with localized adenocarcinoma of the prostate, and prior to any treatment.

Enrollment

361 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patient must have given his/her informed and signed consent
  • The patient must be insured or beneficiary of a health insurance plan
  • Histologically proven presence of prostate adenocarcinoma
  • Localized disease on digital rectal examination
  • Cancer without extensions
  • Acceptance of a curative treatment by the patient

Exclusion criteria

  • The patient is participating in another study
  • The patient is in an exclusion period determined by a previous study
  • The patient is under judicial protection, under tutorship or curatorship
  • The patient refuses to sign the consent
  • It is impossible to correctly inform the patient
  • The patient is taking a hormone-modifying treatment
  • Patient taking adrogenic supplements

Trial design

361 participants in 1 patient group

All study patients
Description:
All patients included according to stated inclusion and exclusion criteria.
Treatment:
Biological: CellSearch detection of the number of circulating, functional, prostate cells
Biological: EPISPOT detection of the number of circulating cells

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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