Chronic kidney disease. Chronic kidney disease (CKD)
Conditions
Interventions
Intervention 1: Intervention group: In the supplement-activity group, the subjects were trained for 8 weeks at the end of each dialysis session (3 sessions per week). Or 24 grams in 150 cc of water wi
Sponsors
University of Sistan and Baluchestan
Eligibility
Sex/Gender
All
Age
25 Years to 55 Years
Inclusion criteria
Inclusion criteria: Hemodialysis 3 times a week Body mass index 35-18/5 kg / m2, At least 6 months on hemodialysis treatment, Absence of severe respiratory and heart failure, chronic inflammatory disease of unknown origin, dementia, cancer, hepatitis B, C, neurological disease, HIV Do not use oral supplements and intravenous nutrition No history of recent surgery in the last quarter Range age 25-55 years
Exclusion criteria
Exclusion criteria: Lack of cooperation of the patient to implement the research protocol, including failure to perform at least two sessions of exercise or lack of supplementation by the patient
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum levels of interleukin-6. Timepoint: Measurement of interleukin-6 levels at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Serum levels of hepcidin. Timepoint: Measurement of hepcidin levels at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Glycemic indexes include fasting blood sugar, insulin and insulin resistance. Timepoint: Measurement at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Lipid profile. Timepoint: Measurement at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Kidney function indicators. Timepoint: Measurement at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Serum iron levels. Timepoint: Measurement at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;Serum ferritin level. Timepoint: Measurement at the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using blood samples with ELISA technique.;The rate of malnutrition. Timepoint: At the beginning of the study and after 8 weeks of protocol implementation. Method of measurement: Using the Malnutrition-Inflammation Questionnaire.;Percentage of body fat. Timepoint: At the beginning of the study and after the end of the study. Method of measurement: Using a caliper. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Sargol Hossein Zadeh
The University of Sistan and Baluchestan
Outcome results
None listed