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Effect of Amygdalus Oil Consumption on Lipid Profile in Patients with Dyslipidemia

Effect of Amygdalus Oil Consumption on Lipid Profile in Patients with Dyslipidemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201411141525N4
Enrollment
80
Registered
2015-02-04
Start date
2014-11-21
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

Hyperlipidemia. Disorders of Llipoprotein Metabolism and Other Lipidaemias

Interventions

Intervention 1: Intervention Group: Use Amygdalus Oil Orally 20 cc per Day for 30 Days. Intervention 2: Control group: No Iintervention.
Treatment - Other
Lifestyle
Intervention Group: Use Amygdalus Oil Orally 20 cc per Day for 30 Days
Control group: No Iintervention

Sponsors

Shiraz University of Medical of Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 20 -70 year old; Low-density Lipoprotein(LDL) 130-169 or Triglyceride 200-400 or High- density Lipoprotein (HDL) Less 50 in Female and Less 40 in Male; Non-use Antilipidemic Drugs; Non History of Renal, Liver, Kidney, Heart, Thyroid, Diabetes mellitus Diseases; Non History of Food Allergy Especially to Amygdalus. Exclusion criteria: Breastfeeding and Pregnancy; Use of Antilipideimic Drugs; Alcohol Consumption; Hospitalization During Study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Low Density Lipoprotein. Timepoint: Before Intervention and One Month After Intervention. Method of measurement: Biochemical Measurements on Blood Sample.;Serum Total Cholesterol. Timepoint: Before Iintervention and One Month After Intervention. Method of measurement: Biochemical Measurements on Blood Sample.;High Density Lipoprotein. Timepoint: Before Intervention and One Month After Intervention. Method of measurement: Biochemical Measurements on Blood Sample.

Secondary

MeasureTime frame
Serum Triglyceride. Timepoint: Before Intervention and One Month After Intervention. Method of measurement: Biochemical Measurements on Blood Sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParham Ostovan

Shiraz University of Medical Sciences

parham.ostovan@yahoo.com+98 71 3628 1561

Outcome results

None listed

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