Impact of an Optimized Omega-3 Formulation on Inflammation and Endothelial Dysfunction in Pulmonary Arterial Hypertension

ConditionPAH
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorUniversity Hospital, Strasbourg, France

About this trial

The objective of this research project is to evaluate the biological effects of long-chain omega-3 supplementation, administered in an optimized, high-purity formulation (EPA:DHA 6:1, \>95% v/v), as an adjunct to standard-of-care treatment in patients with pulmonary arterial hypertension (PAH).

The expected results are confirmation in humans of our preliminary data, namely a beneficial effect on systemic inflammation and pulmonary endothelial dysfunction in PAH. If our hypothesis is confirmed, omega-3s could constitute a complementary nutritional approach to current PAH therapies, subsequently requiring validation through a larger-scale, randomized, controlled study.

Eligibility criteria

Qualifiers

Men or women between the ages of 18 and 75;

Idiopathic, hereditary, drug-induced, or anorexigen-induced PAH, or PAH associated with connective tissue disease;

Stable PAH treatment for at least 90 days;

Subjects capable of understanding the objectives and risks associated with the study and of providing dated and signed informed consent;

Disqualifiers

Patients treated with Omacor®;

Daily consumption of fish oil or fish oil-based dietary supplements (omega-3);

Hypersensitivity or allergy to fish, shellfish, peanuts, soy, corn oil, or coconut oil;

Anticoagulant therapy at therapeutic doses;

Trial design

Treatments tested in this trial

  • OMega 3

Treatment groups

22 Participants
are divided into 1 treatment group

Locations

This trial has no locations