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Rheum palmatum root in systolic heart failure

Clinical trial of the effect of "Rheum palmatum root"on quality of life in patients with systolic heart failure

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180206038645N1
Enrollment
60
Registered
2018-03-05
Start date
2018-04-04
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systolic heart failure. Systolic (congestive) heart failure

Interventions

Intervention 1: Intervention group: Dry extract of Rheum palmatum root with a concentration of 10% relative to 100 gr of roots of the plant, has been standardized 250mg per capsule at the school of ph

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

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

MeasureTime 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

MeasureTime 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

Public ContactZohre Gholami

Zanjan University of Medical Sciences

gholami1393@zums.ac.ir+98 24 3377 0801

Outcome results

None listed

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