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The Effect of DASH Diet on Coagulation Factors, Liver Enzymes, Fibrosis and Steatosis Score and Metabolic Biomarkers in Children with Hemophilia

The Effect of DASH Diet on Coagulation Factors, Liver Enzymes, Fibrosis and Steatosis Score and Metabolic Biomarkers in Children with Hemophilia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130903014551N6
Enrollment
40
Registered
2020-05-26
Start date
2020-06-06
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Hemophilia patient. Acquired hemophilia

Interventions

Intervention 1: Intervention group: Get a DASH diet in the form of diet plans written for 10 weeks and explain the program and replacement list for patients for 3 training sessions, get food record on

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: The desire to participate in the study Male gender Suffering from hemophilia Age ranges between 10-18 years Do not use antioxidant supplements for 3 months before the intervention Do not use a special diet

Exclusion criteria

Exclusion criteria: Smoking and alcohol consumption Use of antihypertensive drugs, blood sugar and blood lipids Having liver, heart and kidney diseases

Design outcomes

Primary

MeasureTime frame
Prothrombin test. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;ALT ?AST. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;Degree of liver fibrosis and steatosis. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Fibrosaccan device.;Fasting blood sugar. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;Lipid profiles. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;Complete blood count. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;Anthropometric measurements. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Body analysis machine.;Systolic and diastolic blood pressure. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Sphygmomanometer.;Weightand height. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Digital scales and tape measure.;Waist circumference. Timepoint: Before and 10 weeks after the intervention. Method of measurement: tape measure.;Hs-CRP. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.;Interleukin 6. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.

Secondary

MeasureTime frame
Vitamin C. Timepoint: Before and 10 weeks after the intervention. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtena Mahdavi

Esfahan University of Medical Sciences

atena.mahdavi2011@yahoo.com+98 31 3673 4658

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 17, 2026