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Effects of vaccinium arctostaphylos fruit on cardiometabolic indices in hypertensive obese patients

Phase 2
Recruiting
Conditions
Condition 1: Obesity. Condition 2: Hypertension.
Obesity due to excess calories
Essential (primary) hypertension
Registration Number
IRCT201710302288N12
Lead Sponsor
Vice Chancellor for Research, Research Institute for Islamic and Complementary Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Iranian male and female hypertensive obese outpatients; patients aged 30 to 80 years; patients with body mass index between 25 kilograms per square meter and 35 kilograms per square meter; patients with systolic blood pressures between 14 and 16 mmHg; patients with diastolic blood pressures between 8 and 10 mmHg; patients taking synthetic antihypertensive drugs with 2 different mechanisms. Exclusion criteria: Patients taking other drugs effective on the blood glucose and lipid levels and body weight; patients with cardiac, renal, hepatic, hematological diseases, hypothyroidism, tachycardia, vertigo and seizure; patients with a history of gallstones or gall bladder surgery; pregnant women; women planning pregnancy; breast-feeding women.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood level of glycosylated hemoglobin. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood level of low density lipoprotein cholesterol. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Body mass index. Timepoint: Before and after 3 months of intervention. Method of measurement: Scale and tape measure.;Waist circumference. Timepoint: Before and after 3 months of intervention. Method of measurement: Tape measure.;Systolic blood pressure. Timepoint: Before and after 3 months of intervention. Method of measurement: 24-hour ambulatory blood pressure monitoring.;Diastolic blood pressure. Timepoint: Before and after 3 months of intervention. Method of measurement: 24-hour ambulatory blood pressure monitoring.
Secondary Outcome Measures
NameTimeMethod
Fasting blood glucose level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood total choletserol level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood triglyceride level. Timepoint: Before and after 3 months of intervention. Method of measurement: kit.;Blood high density lipoprotein cholesterlol level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood serum glutamate oxaloacetate transaminase level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood serum glutatamate pyruvate transaminase level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.;Blood creatinine level. Timepoint: Before and after 3 months of intervention. Method of measurement: Kit.
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