Systolic heart failure. Systolic (congestive) heart failure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Informed study participation Age 40 to 75 Systolic heart failure with ejection fraction equal or lesser than 40 percent Continuing heart medications prescribed by cardiologist
Exclusion criteria
Exclusion criteria: Pregnancy Breast feeding Malignancy Hypersensivity to rheum palmatum root Unwillingness of the patient to continue coperation Chronic Inflamatory diseas Severe Renal failure Collagen vascular disease Sever liver disease Acute infectious disease De compensated heart failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life Score in the Minnesota Questionnaire. Timepoint: Measure the quality of life score at the beginning of study(before intervention)and one week after taking the Rheum Palmatum Root Extract. Method of measurement: Minnesota Living With Heart Failure Questionnaire.;The distance traveled in six minute walk test. Timepoint: Measure the distance traveled in six minute walk test at the beagining of study(before intervention)and one week after taking the Rheum Palmatum Root Extract. Method of measurement: Six minute walk test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Left ventricular ejection fraction. Timepoint: Measurement of left ventricular ejection fraction at the beginning of study (before intervention). Method of measurement: Ecocardiography.;Complete blood count. Timepoint: Measurement of complete blood count at the begining of study(before intervention)and one week after taking Rheum Palmatum Root Extract. Method of measurement: Blood test.;Cr. Timepoint: Measurement of creatinine at the beginning of study (be a for intervention) and one week after taking Rheum palmatum root extract. Method of measurement: Blood test.;ALT. Timepoint: Measurement of Alanin Aminotransfers at the beginning of first study (be a for intervention) and one week after taking Rheum palmatum root extract. Method of measurement: Blood test.;AST. Timepoint: Measurement of Aspartat Aminotransferas at the begining first study (be a for intervention) and one week after taking Rheum palmatum root extract. Method of measurement: Blood test.;CRP. Timepoint: Measurement of C_Reactive Protein at the beginning of first study (be a for intervention) and one week after taking Rheum palmatum extract. Method of measurement: Blood test.;ALKP. Timepoint: Measurement of Alkaline phosphatas at the beginning of study (be a for intervention) and one week after taking Rheum palmatum extract. Method of measurement: Blood test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Zanjan University of Medical Sciences