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Synbiotic Dessert Fortified with Vitamin D and Calcium in Hemodialysis Patients

Effect of Synbiotic Dessert Fortified with Vitamin D and Calcium on Nutritional Indices, Inflammation, Oxidative stress, Malnutrition and Quality of Life in Hemodialysis Patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100223003408N5
Enrollment
42
Registered
2019-04-06
Start date
2018-08-23
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Hemodialysis. Chronic kidney disease, stage 5, End stage kidney disease: on dialysis

Interventions

Intervention 1: Intervention group: 50 gramme of fortified dessert per day for 2 months. Intervention 2: Control group: 50 gramme of placebo dessert for 2 months.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients who are on dialysis more than 6 months Patients with KT/V > 1.2 Patients who are vigilant and can-do Who are on special regiment for dialysis patients Patients who did not have any changes in their recieved erythropoitin for a month

Exclusion criteria

Exclusion criteria: Patients with diabetes, cancer, malignity and autoimmune diseases Patients who are sensitive to dairy products Patients who are grafted and grafted kidney is in their body Patients with vitamin D level more than 70

Design outcomes

Primary

MeasureTime frame
Malondialdehyde (MDA). Timepoint: Before and 60 days after intervention. Method of measurement: Spectrophotometry.

Secondary

MeasureTime frame
Malnutrition-inflammation score. Timepoint: Before and 60 days after intervention. Method of measurement: Questionnaire.;Subjective global assessment. Timepoint: Before and 60 days after intervention. Method of measurement: Questionnaire.;Quality of life. Timepoint: Before and 60 days after intervention. Method of measurement: Questionnaire.;Vitamin D. Timepoint: Before and 60 days after intervention. Method of measurement: ELISA.;Total antioxidant capacity. Timepoint: Before and 60 days after intervention. Method of measurement: ELISA.;HsCRP. Timepoint: Before and 60 days after intervention. Method of measurement: ELISA.;CBC. Timepoint: Before and 60 days after intervention. Method of measurement: Cell counter.;Sodium. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Potasium. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Phosphor. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Calcium. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Albumin. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Cratinine. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Urea. Timepoint: Before and 60 days after intervention. Method of measurement: Autoanalyser.;Ferritin. Timepoint: Before and 60 days after intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Ekramzade

Shiraz University of Medical Sciences

m_ekramzade@yahoo.com+98 71 3725 1001

Outcome results

None listed

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