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Effect of Cornus mas L. on Cardiovascular disease in children

Effect of Cornus mas L. on Inflammatory Risk Factors, Lipid Profile and Apolipoproteins in Dyslipidemic Children

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206109662N3
Enrollment
40
Registered
2012-09-16
Start date
2011-08-29
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

dyslipidemia. Endogenous hyperglyceridaemia Fredrickson's hyperlipoproteinaemia, type IV Hyperlipidaemia, group B Hyperprebetalipoproteinaemia Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinaemia

Interventions

Intervention 1: case group: using 50 g of CM twice a day after the lunch and dinner. Intervention 2: case group:no treatment.
Prevention
Treatment - Drugs
case group: using 50 g of CM twice a day after the lunch and dinner

Sponsors

Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to 16 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: subjects that had at least one of the dyslipidemic measures such as TG (=150 mg/dL), TC (=170 mg/dL), LDL (=130 mg/dL) and low HDL (<35 mg/dL) in serum; dyslipidemic children between the ages of 9-16 years. Exclusion criteria: known diabetes mellitus; liver disease; nephrotic syndrome; thyroid disorders; chronic pancreatitis; bile duct disorders; the use of medication that would alter lipid metabolism; the informed consent not being signed.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Total cholesterol. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: spectrophotometeric method.;Low-density lipoprotein. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: Friedewald formula.;High-density lipoprotein. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: spectrophotometeric method.;Triglyceride. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: spectrophotometeric method.

Secondary

MeasureTime frame
WHR. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: tape.;BMI. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: tape.;VCAM. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: ELISA kit.;ICAM. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: ELISA kit.;CRP. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: automated chemistry analyzer.;Apo A. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: automated chemistry analyzer.;Apo B. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: automated chemistry analyzer.;HDL/LDL. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: spectrophotometeric method.;HDL/TC. Timepoint: baseline and after the 3 and 6 wk of the treatment. Method of measurement: spectrophotometeric method.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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