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Clinical Trials/JPRN-UMIN000015141
JPRN-UMIN000015141
Completed
N/A

A randomized controlled trial for improving blood lipids in human A randomized double-blind parallel-group study - A trial for improving blood lipids

ORTHOMEDICO Inc.0 sites24 target enrollmentJune 1, 2015
ConditionsHealthy adults

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy adults
Sponsor
ORTHOMEDICO Inc.
Enrollment
24
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Fukumoto S, Katsumata Y, Yoshikawa K, Sakaida K, Suzuki N, Yamamoto K, Takara T, Yazawa K. Effect of Supplement Containing Krill Oil on Serum Lipids in Japanese-A Randomized, Double-blind, Placebo-controlled Study-. Jpn Pharmacol Ther. 2015; 43(6): 837-847.

Registry
who.int
Start Date
June 1, 2015
End Date
January 31, 2015
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • a)Persons who have previous medical history of malignant tumor or heart failure or myocardial infarction b)Patients being treated for at least one of following diseases atrial fibrillation, cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension and other chronic disease c)Persons who take medicines, herbal medicines \*Especially, to exclude persons who take anticoagulants, antithrombotic drug (acetylsalicylic acid, warfarin, etc.) d)Persons who are allergic to medicines, or products related to the test material of this trial \*Especially, to exclude persons with gelatin or shellfish allergy because of including gelatin in the capsule film and shrimp essence in the placebo fragrances e)Pregnant women, lactating women, or women who want to get pregnant during the trial period f)Persons who plan an operation g)Persons who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial h)Persons who are judged not suitable to participate in this trial by physician

Outcomes

Primary Outcomes

Not specified

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