Leftover human material for liquid biopsy research.

The use of surplus human material (left-over samples) for the design, validation and (further) development of liquid diagnostics tests. - Leftover human material for liquid biopsy research.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON57893

Enrollment

3000

Registered

2025-02-06

Start date

2025-10-29

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer diagnostics

Interventions

In-house IVD

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients over 18 years of age, mentally competent, who have not stated any objections to the use of leftover material and have or will have leftover material available.

Exclusion criteria

Exclusion criteria: Patients under the age of 18, patients who are not mentally competent and/or patients who have objected to the use of leftover material.

Design outcomes

Primary

Measure	Time frame
Completed development of the ‘liquid diagnostics’ tests and/or clinical validation and implementation of the required tests and body fluids based on current and future guidelines and recommendations.	—

Countries

Netherlands

Contacts

Public ContactR.J. Haastert

St. Antonius Ziekenhuis

r.van.haastert@antoniusziekenhuis.nl0883207683

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 3, 2026