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Effects of Fish Oil on Platelet Function and Coagulation

Effects of Fish Oil on Platelet Function and Coagulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03048981
Acronym
FOILP
Enrollment
12
Registered
2017-02-09
Start date
2017-03-01
Completion date
2017-05-02
Last updated
2017-05-09

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

Conditions

Atherosclerosis, Platelet Aggregation, Spontaneous, Surgery

Keywords

Thrombocyte aggregation, Fish oil, Alternative medicine, Point of care testing, Coagulation monitoring

Brief summary

Many patients undergoing surgery use naturopathic drugs, including fish oil. Fish oil has been reported to increase bleeding in patients through inhibiting platelet aggregation and prolonging of clot formation time. The Swedish Medical Products Agency recommends that patients stop taking the naturopathic medicines including fish oil two weeks prior planed surgery. The aim of this study is to examine the effects of fish oil given to healthy volunteers using point of care coagulation assessment and flow dependent Cellix instrument before and after intake of fish oil.

Detailed description

Healthy volunteers will be given maximum dose of fish oil for 7 days. Blood samples will be collected before and immediately after the 7 days of intake and analysed using point of care coagulation assessment instruments and flow dependent platelet aggregation using a microfluid flow controlled system (Cellix). For point of care coagulation assessment the multiple electrode platelet aggregometer Multiplate, the viscoelastic rotational thromboelastometers ROTEM and Sonoclot will be used. Flow cytometry may also be utilized.

Interventions

DRUGFish oil

Blood samples before and after 10 day intake of maximum dose fish oil

Sponsors

Region Skane
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Before and after

Eligibility

Sex/Gender
ALL
Age
19 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Non smoking healthy volunteers with written consent to participate

Exclusion criteria

* Medication affecting coagulation or platelets within 14 days priori to inclusion

Design outcomes

Primary

MeasureTime frameDescription
Thrombocyte aggregation measured with multiple electrode aggregometryChange of thrombocyte aggregation directly after intake period of 7 days compared to baselineMultiple electrode aggregometry gives a area under the curve proportional to thrombocyte aggregation
Thrombocyte aggregation measured with Cellix's microfluidic pumps and biochipsChange of thrombocyte aggregation directly after intake period of 7 days compared to baselineCellix's microfluidic pumps and biochips gives an thrombosis area proportional to thrombocyte aggregation

Secondary

MeasureTime frameDescription
Coagulation measured with the viscohemostatic instrument ROTEMChange of coagulation directly after intake period of 7 days compared to baselineViscohemostatic instrument
Coagulation measured with the viscohemostatic instrument and SonoclotChange of coagulation directly after intake period of 7 days compared to baselineViscohemostatic instrument

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026