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Evaluation of effects of pomegeranate seed oil on lipid profiles, apolipoproteines and body composition in subjects with low HDL-C concentrations

Evaluation of effects of pomegeranate seed oil on lipid profiles, apolipoproteines and body composition in subjects with low HDL-C concentrations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107201640N5
Enrollment
150
Registered
2011-09-29
Start date
2011-04-16
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

low HDL-C concentrations. Disorders of lipoprotein metabolism and other lipidaemias

Interventions

Intervention 1: The 1600 mg PSO group: 2 PSO (800 mg PSO) capsules and 2 placebo capsules. Intervention 2: The 3200 mg PSO group: 4 PSO capsules daily. Intervention 3: Control group: 4 placebo capsule
Treatment - Other
Treatment - Drugs
Placebo
The 1600 mg PSO group: 2 PSO (800 mg PSO) capsules and 2 placebo capsules.
The 3200 mg PSO group: 4 PSO capsules daily.
Control group: 4 placebo capsules.

Sponsors

Research Institute for Endocrine Science, Shaheed Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to cooperate; ages 20-70 years; those with 35= BMI (kg/m2) =25; having levels of HDL-C 10Kg during the study, Diagnosis of any of the diseases mentioned in inclusion criteria, during the study; Patient's lack of cooperation in each of the stages studied.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Low HDL-C. Timepoint: baseline and end of weeks 2, 4, 8 and 12. Method of measurement: Enzymatic colorimetric method and sediment specific.

Secondary

MeasureTime frame
Body weight. Timepoint: at the start and end of the 12 weeks study. Method of measurement: anthropometric measurements.;Blood pressure. Timepoint: at the start and end of the 12 weeks study. Method of measurement: blood pressure measurement.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvin Mirmiran

Obesity Research Center, Research Institue for Endocrine Science, Shaheed Beheshti University of Med

mirmiran@endocrine.ac.ir+98 21 2243 2500

Outcome results

None listed

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