| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000023667 |
| Receipt No. | R000027261 |
| Official scientific title of the study | The verification study for the blood lipid reduction effects of garlic egg yolk: a randomized, double-blind, controlled trial |
| Date of disclosure of the study information | 2017/07/28 |
| Last modified on | 2017/02/01 (Ver. 4) |
| Basic information | ||
| Official scientific title of the study | The verification study for the blood lipid reduction effects of garlic egg yolk: a randomized, double-blind, controlled trial | |
| Title of the study (Brief title) | The verification study for the blood lipid reduction effects of garlic egg yolk | |
| Region |
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| Condition | |||
| Condition | Healthy adults | ||
| Classification by specialty |
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| Classification by malignancy | Others | ||
| Genomic information | NO | ||
| Objectives | |
| Narrative objectives1 | To verify the blood lipid reduction effects due to the ingestion of the test food. |
| Basic objectives2 | Safety,Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | Exploratory |
| Trial characteristics_2 | Explanatory |
| Developmental phase | Not applicable |
| Assessment | |
| Primary outcomes | 1. LDL-cholesterol
*1 Take the blood samples at 0 week and at 6 and 12 weeks after the ingestion |
| Key secondary outcomes | 1. Total cholesterol, HDL-cholesterol, LDL/HDL ratio, Neutral fat (triglyceride: TG), Free fatty acid, MDA-LDL
*1 Take the blood samples at 0 week and at 6 and 12 weeks after the ingestion 2. Body weight, BMI, Body fat percentage *2 Take the measurements at 0 week and at 6 and 12 weeks after the ingestion |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Parallel |
| Randomization | Randomized |
| Randomization unit | Individual |
| Blinding | Double blind -all involved are blinded |
| Control | Placebo |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 2 | |
| Purpose of intervention | Treatment | |
| Type of intervention |
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| Interventions/Control_1 | Duration: 12 weeks
Test material:"Garlic egg yolk 229-55 ninnikugogo" Dose: Take one capsule, three times a day Administration: Take one capsule after each meal |
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| Interventions/Control_2 | Duration: 12 weeks
Test material: Placebo Dose: Take one capsule, three times a day Administration: Take one capsule after each meal |
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| Interventions/Control_3 | ||
| Interventions/Control_4 | ||
| Interventions/Control_5 | ||
| Interventions/Control_6 | ||
| Interventions/Control_7 | ||
| Interventions/Control_8 | ||
| Interventions/Control_9 | ||
| Interventions/Control_10 | ||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1. LDL-cholesterol level was high in the most recent health diagnosis | |||
| Key exclusion criteria | 1. At least one previous medical history of malignant tumor, heart failure or myocardial infarction
2. Currently under the treatment for either cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension or other chronic diseases 3. Currently taking medicines and/or herbal medicines 4. Allergic to medicines or foods related to the test food of this trial 5. Pregnant, lactating, or planning to get pregnant during the trial period 6. Enrolled into other clinical trials within the last 3 months before agreeing to participate in this trial 7. Judged unsuitable for participating in this trial by physician |
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| Target sample size | 50 | |||
| Research contact person | |
| Name of lead principal investigator | Kazuo YAMAMOTO |
| Organization | ORTHOMEDICO, Inc. |
| Division name | R&D Department |
| Address | 2F Sumitomo Fudosan Korakuen Bldg., 1-4-1 Koishikawa, Bunkyo-ku, Tokyo. |
| TEL | 03-3818-0610 |
| kazu@orthomedico.jp | |
| Public contact | |
| Name of contact person | Naoko SUZUKI |
| Organization | ORTHOMEDICO, Inc. |
| Division name | R&D Department |
| Address | 2F Sumitomo Fudosan Korakuen Bldg., 1-4-1 Koishikawa, Bunkyo-ku, Tokyo. |
| TEL | 03-3818-0610 |
| Homepage URL | |
| nao@orthomedico.jp | |
| Sponsor | |
| Institute | ORTHOMEDICO, Inc. |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Temahimado Co., Ltd. |
| Organization | |
| Division | |
| Category of Funding Organization | Profit organization |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | 1. Seishin-kai Medical Association Inc, Takara Medical Clinic.
2. Evaluation Center of Health and Nutrition Inc. |
| Name of secondary funder(s) | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | 医療法人社団 盛心会 タカラクリニック (東京都)
Seishin-kai Medical Association Inc, Takara Medical Clinic (Tokyo) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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| Anticipated trial start date |
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| Last follow-up date | |||||||
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| Related information | |
| URL releasing protocol | |
| Publication of results | Published |
| URL releasing results | |
| Results | Suzuki N, Yamamoto K, Kakino K, Takara T. The Effects of Administration of Garlic-egg Yolk-containing Supplements on Serum Lipid Level in Humans -A Randomized, Double-blind, Placebo-controlled Trial-. Jpn Pharmacol Ther. 2016; 44(11): 1645-1653. |
| Other related information | |
| Management information | |||||||
| Registered date |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027261 |