Healthy Clinical Trial
Official title:
Effect of Omega-3 Index on Cellular Metabolism and Quality of Life Following the Administration of a Customized Dose of Omega-3 Oil
| Verified date | October 2018 |
| Source | SCF Pharma |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Determine whether personal optimization of the Omega-3 index improves cellular metabolism and quality of life (according to the SF-36 form).
| Status | Completed |
| Enrollment | 16 |
| Est. completion date | March 14, 2019 |
| Est. primary completion date | March 14, 2019 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 19 Years and older |
| Eligibility |
Inclusion Criteria: - Participant aged 19 or over - Available for the entire duration of the study and willing to participate on the basis of the information provided in the FIU duly read and signed. Exclusion Criteria: - Allergy known to fish - Pregnant women who breast-feed or test positive for pregnancy |
| Country | Name | City | State |
|---|---|---|---|
| Canada | SCF Pharma | Rimouski | Quebec |
| Lead Sponsor | Collaborator |
|---|---|
| SCF Pharma | Université du Québec à Rimouski |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Omega-3 Index | Achievement of an omega-3 index of 8. | 8 weeks | |
| Secondary | Cellular metabolism | To determine whether the achievement of the optimal level of the omega-3 index results in an improvement in the white blood cell energy metabolism | 8 weeks | |
| Secondary | Quality of life | Determine whether the achievement of the optimal level of the Omega-3 index results in an improvement in quality of life (according to Form SF-36) | 8 weeks | |
| Secondary | Heart rate | Confirm the link between the optimal omega-3 index and heart rate (bpm) | 8 weeks | |
| Secondary | Total Cholesterol | Confirm the link between the optimal omega-3 index and total cholesterol (in mmol/L) | 8 weeks | |
| Secondary | Triglycerides | Confirm the link between the optimal omega-3 index and triglycerides level (in mmol/L) | 8 weeks | |
| Secondary | HDL-cholesterol | Confirm the link between the optimal omega-3 index and HDL-cholesterol (in mmol/L) | 8 weeks | |
| Secondary | LDL-cholesterol | Confirm the link between the optimal omega-3 index and LDL-cholesterol (in mmol/L) | 8 weeks | |
| Secondary | Alanine aminotransferase | Confirm the link between the optimal omega-3 index and alanine aminotransferase (in U/L | 8 weeks | |
| Secondary | Aspartate aminotransferase | Confirm the link between the optimal omega-3 index and aspartate aminotransferase (in U/L) | 8 weeks | |
| Secondary | Bilirubin | Confirm the link between the optimal omega-3 index and Bilirubin (in µmol/L) | 8 weeks | |
| Secondary | Albumin | Confirm the link between the optimal omega-3 index and Albumin (in g/L) | 8 weeks | |
| Secondary | C-reactive protein | Confirm the link between the optimal omega-3 index and C-reactive protein (in mg/L) | 8 weeks | |
| Secondary | Apolipoprotein B | Confirm the link between the optimal omega-3 index and Apolipoprotin B (in mmol/L) | 8 weeks | |
| Secondary | Erythrocyte sedimentation rate | Confirm the link between the optimal omega-3 index and the erythrocyte sedimentation rate (in min) | 8 weeks | |
| Secondary | Systolic blood pressure | Confirm the link between the optimal omega-3 index and the systolic blood pressure (in mm Hg) | 8 weeks | |
| Secondary | Diastolic blood pressure | Confirm the link between the optimal omega-3 index and the diastolic blood pressure (in mm Hg) | 8 weeks |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT06052553 -
A Study of TopSpin360 Training Device
|
N/A | |
| Completed |
NCT05511077 -
Biomarkers of Oat Product Intake: The BiOAT Marker Study
|
N/A | |
| Recruiting |
NCT04632485 -
Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
|
||
| Completed |
NCT05931237 -
Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults
|
N/A | |
| Terminated |
NCT04556032 -
Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women
|
N/A | |
| Completed |
NCT04527718 -
Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT04998695 -
Health Effects of Consuming Olive Pomace Oil
|
N/A | |
| Completed |
NCT04065295 -
A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225
|
Phase 1 | |
| Completed |
NCT04107441 -
AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects
|
Phase 1 | |
| Completed |
NCT01442831 -
Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
|
Phase 1 | |
| Terminated |
NCT05934942 -
A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood
|
Phase 1 | |
| Recruiting |
NCT05525845 -
Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI
|
N/A | |
| Completed |
NCT05515328 -
A Study in Healthy Men to Test How BI 685509 is Processed in the Body
|
Phase 1 | |
| Completed |
NCT04967157 -
Cognitive Effects of Citicoline on Attention in Healthy Men and Women
|
N/A | |
| Completed |
NCT05030857 -
Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects
|
Phase 1 | |
| Recruiting |
NCT04494269 -
A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls
|
Phase 1 | |
| Recruiting |
NCT04714294 -
Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT04539756 -
Writing Activities and Emotions
|
N/A | |
| Recruiting |
NCT04098510 -
Concentration of MitoQ in Human Skeletal Muscle
|
N/A | |
| Completed |
NCT03308110 -
Bioavailability and Food Effect Study of Two Formulations of PF-06650833
|
Phase 1 |