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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02092584
Other study ID # 5144
Secondary ID
Status Completed
Phase Phase 4
First received March 18, 2014
Last updated March 18, 2014
Start date December 2011
Est. completion date October 2013

Study information

Verified date March 2014
Source Tehran University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of this study is the comparison between the effects of supplementation with omega 3 or placebo for 8 weeks in serum level of IGF-1 and IGFBP-3 and gene expression of IGF-1 in patients with cardiovascular disease.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date October 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Male
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria:

- CVD patients 45- 65 years old, patients with = 50% stenosis in at least one coronary angiogram demonstrated, body mass index in the range 18.5- 35, avoidance of dietary supplements, vitamins and herbal products at least 3 months before and throughout the intervention, willingness to participation,

Exclusion Criteria:

- people who have used omega 3 supplements in last 3 months, having chronic renal disease , GI disease, hepatobiliary diseases, hematological disorders, hypo- or hyperthyroidism, Smokers

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Omega-3
4 cap 1 g Omega-3 per day for 2 months
Placebo
4 cap 1 g Placebo(paraffin) per day for 2 months

Locations

Country Name City State
Iran, Islamic Republic of Tehran University of Medical Sciences Tehran

Sponsors (1)

Lead Sponsor Collaborator
Tehran University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum Total Cholesterol Change from baseline at 2 months No
Primary Serum HDL-C Change frome baseline at 2 months No
Primary Serum LDL-C Change frome baseline at 2 months No
Primary Serum TG Change frome baseline at 2 months No
Primary Serum Fasting Blood Sugar(FBS) Change frome baseline at 2 months No
Primary Serum Insulin Change frome baseline at 2 months No
Primary Serum hsCRP Change frome baseline at 2 months No
Primary Serum Insulin Like Growth Factor-1(IGF-1) Change frome baseline at 2 months No
Primary Serum IGF binding protein 3(IGFBP-3) Change frome baseline at 2 months No
Secondary Gene Expression of IGF-1 Change frome baseline at 2 months No
Secondary Gene expression of IGFBP3 change from baseline at 2 months No
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