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Blood Sampling of Healthy Volunteers for Immunological Research

Netherlands Cancer Institute (NKI) logo

Netherlands Cancer Institute (NKI)

Status

Enrolling

Conditions

Healthy Volunteers

Treatments

Other: Blood sample

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This protocol will be used to collect crucial components of the immune system from healthy volunteers for the characterization of immune cells in fresh blood. A pipeline has been set up for comprehensive immune phenotyping of both lymphoid and myeloid cells within 24 hours after blood withdrawal.

Full description

In order to properly compare the immunobiology of healthy volunteers to (advanced) cancer patients, the investigators use age-matched controls with no history of cancer and no potentially interfering medication.

Healthy volunteers will be asked to donate 5 tubes of blood

Enrollment

50 estimated patients

Sex

All

Ages

36+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age above 35 years
  • Written informed consent
  • No history of cancer
  • No use of systemic immunosuppressive medication (eg. corticosteroids). Local use of corticosteroids (eg. topical or inhalation) is allowed.

Exclusion criteria

  • Fever 14 days before blood withdrawal
  • Donated blood for the same program within the last 2 years
  • Pregnancy

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Blood sample
Other group
Description:
Blood sample
Treatment:
Other: Blood sample

Trial contacts and locations

1

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Central trial contact

L Voorwerk, MD; M Kok, MD

Data sourced from clinicaltrials.gov

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