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The effect of sesame lignans on atherosclerosis

The effect of sesame lignans consumption on carotid intima-media thickness, serum endothelial markers, some angiogenic mediators gene expression in patients candidated for angiography

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201709246722N2
Enrollment
40
Registered
2017-11-04
Start date
2016-08-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Atherosclerosis. Condition 2: Atherosclerosis. Condition 3: Atherosclerosis. Condition 4: Atherosclerosis. Condition 5: Atherosclerosis. Condition 6: Atherosclerosis. Condition 7: Atherosclerosis. Condition 8: Atherosclerosis. Atherosclerosis of aorta Atherosclerosis of other arteries Generalized and unspecified atherosclerosis Dissection of aorta [any part] Aneurysm and dissection of carotid artery Disorder of arteries and arterioles, unspecified Peripheral angiopathy in dis

Interventions

Intervention 1: placebo capsule containing starch one capsule per day 10 weeks. Intervention 2: sesame lignans each capsule containing 500 mg one capsule per day 10 weeks.
Placebo
Prevention
placebo capsule containing starch one capsule per day 10 weeks
sesame lignans each capsule containing 500 mg one capsule per day 10 weeks

Sponsors

Vice chancello for research,Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:40 to 70 years old ; candidate for angiography; Carotid Intima-media thickness more than standard (0.8 mm); patients voluntarily confirm their willingness to participate in the study Exclusion criteria: MI or illness associated with artery clogging which is untreated; any change in the amount or type of medications consumed during intervention; inflammatory disease require NSAIDs medications; lack of desire to continue the collaboration;not taking 10 percent of supplements (not to use for one week); the incidence of allergic reaction to supplement; obesity (body mass index of 35 and more); comorbidity of a chronic disease (renal or hepatic insufficiency, pulmonary failure, a history of cancer or asthma); the use of NSAIDs; usage of dietary/ herbal /multi-vitamin supplements at least two weeks before the start of the intervention

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Carotid Intima-media thikness. Timepoint: before and after intervention. Method of measurement: color dopler ultrasonography.;VEGF serum concentration. Timepoint: before and after intervention. Method of measurement: ELISA assay.;ICAM1 serum concentration. Timepoint: before and after intervention. Method of measurement: ELISA assay.;VCAM1 serum concentration. Timepoint: before and after intervention. Method of measurement: ELISA assay.;VWF serum concentration. Timepoint: before and after intervention. Method of measurement: ELISA assay.;HsCRP serum concentration. Timepoint: before and after intervention. Method of measurement: ELISA assay.;VEGF gene expression. Timepoint: before and after intervention. Method of measurement: qRTPCR.;ICAM1 gene expression. Timepoint: before and after intervention. Method of measurement: qRTPCR.;Gamma INF gene expression. Timepoint: before and after intervention. Method of measurement: qRTPCR.

Secondary

MeasureTime frame
Systolic blood pressure. Timepoint: before and after intervention. Method of measurement: medical barometer.;Serum FBS concentration. Timepoint: before and after intervention. Method of measurement: enzymatic kit.;Serum HDLc concentration. Timepoint: before and after intervention. Method of measurement: enzymatic kit.;Serum TG concentration. Timepoint: before and after intervention. Method of measurement: enzymatic kit.;Serum total colesterol concentration. Timepoint: before and after intervention. Method of measurement: enzymatic kit.;Serum LDLc concentration. Timepoint: before and after intervention. Method of measurement: enzymatic kit.;Diastolic blood pressure. Timepoint: before and after intervention. Method of measurement: medical barometer.;Weight. Timepoint: before and after intervention. Method of measurement: medical scale.;Waist circumference. Timepoint: before and after intervention. Method of measurement: measuring tape.;Hip circumference. Timepoint: before and after intervention. Method of measurement: measuring tape.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Mokhber

Tehran University of Medical Sciences

"marmokhber@razi.tums.ac.ir ; m.mokhber@chmail.ir+98 21 8889 2209

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026