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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03251014
Other study ID # 06-01-04-SF2310
Secondary ID NMRR-16-2693-323
Status Completed
Phase N/A
First received May 30, 2017
Last updated August 14, 2017
Start date October 2016
Est. completion date May 9, 2017

Study information

Verified date August 2017
Source Universiti Putra Malaysia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed to determine the thrombotic effects of YSS compared with salmon among healthy overweight subjects. It hypothesized that YSS may result significant, favorable thrombotic effects and the effects may be similar with salmon.


Description:

The project was a randomized, two-period, crossover trial with 8-week treatment periods and 8-week washout period. A total of 50 healthy overweight adults were recruited among staff and students in UPM. All the subjects were randomized into two groups. Each group was served with either cooked YSS (~265 g/ day) or salmon (~246 g/day) thrice per week. Blood and urine samples were collected for laboratory assessment.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date May 9, 2017
Est. primary completion date May 9, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 55 Years
Eligibility Inclusion Criteria:

- Malaysian

- Overweight participants (BMI 23-27.4 kg/m2)

Exclusion Criteria:

- Regular use of fish oil supplements during the last one month

- Regular consumption of fish twice or more per week

- Vegetarian who excluded all meat, fish, and poultry from their diet

- Diagnosed with cardiovascular disease, haemostasis disorder, inflammatory disease, diabetes mellitus, hypertension, or other significant medical history that may prohibits the participation

- Receiving warfarin or aspirin treatment, or medication to lower serum lipids, blood pressure, and inflammation

- Women who are menopause, pregnant or lactating

Study Design


Related Conditions & MeSH terms


Intervention

Other:
YSS
Intervention providing steamed whole YSS (~265 g/day, 3 days/week) for eight weeks
Salmon
Intervention providing steamed salmon fillet (~246 g/day, 3 days/week) for eight weeks

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Universiti Putra Malaysia Ministry of Science, Technology and Innovation (MOSTI) Malaysia

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in hemostatic status assessed by immunoassay method Hemostatic markers including vWF-A2 and CD62b (p-selectin) in pg/mL are evaluated. 8 weeks
Secondary Changes in lipid and glucose profiles analysed by medical diagnostic laboratory Total cholesterol, triglyceride, HDL-cholesterol, LDL-cholesterol, VLDL-cholesterol, and fasting blood glucose in mmol/L are evaluated. 8 weeks
Secondary Changes in liver enzymes analysed by medical diagnostic laboratory Serum levels of alanine transaminase (ALT), aspartate transaminase (AST), alkaline Phosphatase (ALP) and gamma glutamyl transferase (GGT) in IU/L are determined. 8 weeks
Secondary Changes in renal function analysed by medical diagnostic laboratory Serum levels of creatinine, urea, and electrolytes (sodium, potassium, and chloride) in mmol/L are determined. 8 weeks
Secondary Changes in body mass index (BMI) Weight and height are combined to report BMI in kg/m^2 8 weeks
Secondary Changes in blood pressure Seated systolic and diastolic blood pressures are taken in mmHg. 8 weeks
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