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Effects of isoflavones in peritoneal dialysis patients

Effects of isoflavones on hypertension, serum concentrations of fructoseamine and advanced glycated end products in peritoneal dialysis patients

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091116002716N4
Enrollment
44
Registered
2019-12-22
Start date
2019-11-16
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

End stage of renal disease. Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group: Patients in the isoflavone group receive, for 8 weeks, two tablets of Soyagol (Goldaru Company) per day, each containing 50 mg of soy isoflavone. Intervention 2: Co

Sponsors

National Nutrition and Food Technology Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Continuous Ambulatory Peritoneal Dialysis for 6 months or more Body mass index below 35

Exclusion criteria

Exclusion criteria: infections; inflammatory diseases liver diseases past medical history of cancer receiving glucocorticoid and anti-inflammatory drugs receiving isoflavone supplements Constant consumption of soy or foods containing soy in the diet

Design outcomes

Primary

MeasureTime frame
Serum concentrations of glucose. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: Enzymatic method.;Serum concentrations of fructoseamine. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: The enzyme-linked immunosorbent assay (ELISA).;Serum concentrations of carboxymethyl lysine. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: The enzyme-linked immunosorbent assay (ELISA).;Serum concentrations of pentosidine. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: The enzyme-linked immunosorbent assay (ELISA).;Systolic blood pressure. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: mercury sphygmomanometer.;Diastolic blood pressure. Timepoint: Before the intervention and 8 weeks after the intervention. Method of measurement: mercury sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hadi Tabibi

Faculty of Nutrition and Food Technology, Shahid Beheshti medical university

hadtabibi@yahoo.com+98 21 2207 7424

Outcome results

None listed

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