Obtaining blood from healthy volunteers for assay validation on iron parameters.

Obtaining blood from healthy volunteers for assay validation on iron parameters. - HAVIP

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON46555

Enrollment

Registered

2018-05-17

Start date

2018-06-05

Completion date

Unknown

Last updated

2024-04-15

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

Conditions

Iron disorders Iron disorders

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Participants need to be healthy volunteers between 18 and 55 years old. They should live in the Netherlands and preferably in the area of Nijmegen. People who are diagnosed with any iron disorder can not participate in this study. Examples of Iron disorders are anemia, β-thalassaemia, hemochromatosis and IRIDA. Also people that use any sort of medication can not participate, however the use of contraceptive pills is allowed.

Exclusion criteria

Exclusion criteria: If deviant iron parameter values are found in samples of the healthy volunteers they will be excluded from the study.

Design outcomes

Primary

Measure	Time frame
The main study endpoint for this study is storage of blood from healthy volunteers to use in the validation of an ERFE assay.	—

Secondary

Measure	Time frame
The use of the stored plasma and serum for the validation of assays in the field of iron metabolism in the next 10 years.	—

Countries

Netherlands

Outcome results