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Resistance to chemotherapy induced by plasma from healthy volunteers after fish oil consumption

Resistance to chemotherapy induced by plasma from healthy volunteers after fish oil consumption - Fish Oil Volunteer Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38363
Enrollment
28
Registered
2012-03-15
Start date
2012-04-11
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

het gaat hier om gezonde vrijwilligers zonder aandoening. chemoresistance

Interventions

The intervention is this study is intake of fish or fish oil at T0. Volunteers will be randomly assigned to one of three fish oil brands, or to each of the fish species.

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. The volunteer must be >= 18 years of age 2. The volunteer must be healthy, meaning: * no history of diabetes mellitus * no history of immune disorders * no history of hypercholesterolemia * no use of anti-coagulant medication * no breast feeding * no allergy to fish or related products 3. The patient may not have used fish oil products within 2 weeks before start of the study 4. The patient may not have eaten a fish meal within 1 week before the start of the study 5. The patient must have given written informed consent

Exclusion criteria

Exclusion criteria: Any other condition by which the volunteer does not meet the inclusion criteria.

Design outcomes

Secondary

MeasureTime frame
Secondary endpoint: The ability of plasma withdrawn from volunteers that have ingested fish oil or fish to induce resistance in an in vitro tumor cell culture, or in vivo in mouse models.

Primary

MeasureTime frame
Primary endpoint: To determine the level of 16:4(n-3) in plasma withdrawn from volunteers that have ingested fish oil or fish.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)