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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02908828
Other study ID # 2015/2303
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date September 19, 2017

Study information

Verified date September 2020
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Copepod oil is extracted from the marine copepod Calanus finmarchicus, the dominant plankton species in the marine food web in the Norwegian Sea. Copepods constitute the largest renewable and harvestable resource in the Norwegian Sea and adjacent waters, and it is now developed knowledge and technology for sustainable harvesting of this "new" resource. The purpose of this study is to investigate whether Calanus copepod oil supplementation has an equivalent effect on maximal oxygen uptake in humans to that seen in experimental studies in mice.


Recruitment information / eligibility

Status Completed
Enrollment 71
Est. completion date September 19, 2017
Est. primary completion date September 19, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 50 Years
Eligibility Inclusion Criteria:

- in good health

- Body mass index (BMI) between 18,5 and 29,9

Exclusion Criteria:

- Medical condition limiting VO2max (COPD or asthma).

- diagnosed coronary artery disease

- Any other significant medical condition

- medication effecting exercise capacity (e.i. betablockers)

- Pregnancy

- Participation in other clinical trials

- Shellfish allergies

- Systolic blood pressure > 170 mmHG, or diastolic BP > 105 mmHG.

- contraindications for maximal exercise testing

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Calanus oil

placebo dietary oil


Locations

Country Name City State
Norway Institutt for Medisinsk Biologi, UiT Norges arktiske universitet Tromsø
Norway KG Jebsen-senter for Hjertetrening, NTNU Trondheim

Sponsors (3)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Calanus, University of Tromso

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary maximal oxygen uptake (VO2max) Measured with indirect calorimetry at a treadmill (running/walking) with gradually increasing work load until exhaustion. After 10-15 min with warmup at 70% of maximal heart rate, work load will be increased every 1-2 minute and the changes maximal oxygen uptake (VO2) will be recorded automatically. 6 months
Secondary Body composition (InBody, Japan) 6 months
Secondary Self-reported physical activity assessed with International Physical Activity Questionnaire (IPAQ) short version 6 months
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