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Evaluation the effect of allium hirtifolium in the treatment of hyperlipidemia

Phase 3
Conditions
Hyperlipidemia.
Hyperlipidemia, unspecified
E78.5
Registration Number
IRCT20150721023282N7
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Age of more than 18 years
Serum level of LDL between 100 to 160 mg/dL
Having less than 2 cardiovascular risk factors

Exclusion Criteria

Cardiac stable angina
Diabetes mellitus
Diseases affecting level of serum lipids
Use of drugs affecting level of serum lipids

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of triglycerides. Timepoint: Before the intervention and the end of intervention (6 weeks after the start of intervention). Method of measurement: Blood test.;Serum level of LDL. Timepoint: Before the intervention and the end of intervention (6 weeks after the start of intervention). Method of measurement: Blood test.;Serum level of HDL. Timepoint: Before the intervention and the end of intervention (6 weeks after the start of intervention). Method of measurement: Blood test.;Serum level of total cholesterol. Timepoint: Before the intervention and the end of intervention (6 weeks after the start of intervention). Method of measurement: Blood test.
Secondary Outcome Measures
NameTimeMethod
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