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Pomegranate extract and hemodialysis patients

Evaluating the effect of Pomegranate extract on nutritional status, anemia and inflammatory biomarkers of hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201502225161N2
Enrollment
80
Registered
2016-06-23
Start date
2015-08-06
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

End Stage Renal Disease. Chronic kidney disease, stage 5

Interventions

Intervention 1: Intervention group: 2 g of Pomegranate extract before every dialysis session for 8 weeks. Intervention 2: control group: 4 capsules of placebo before every hemodialysis session.
Treatment - Drugs
Placebo
Intervention group: 2 g of Pomegranate extract before every dialysis session for 8 weeks
control group: 4 capsules of placebo before every hemodialysis session

Sponsors

Vice-Chancellor for Research and Technology Affairs
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ESRD patients on chronic hemodialysis for at least three consecutive months Exclusion criteria: history of hypersensitivity to pomegranate; kidney transplant less than 6 months before study enrollment; vitamin E (60 IU/day or more), vitamin C (500 mg/day or more), or other antioxidant supplements during the month before the study; history of hospitalization during 3 months before the study; patients with life-threatening comorbidities including malignancies; being severely deconditioned

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
CRP. Timepoint: before and after the intervention. Method of measurement: blood sample.;Hemoglobin. Timepoint: before and after the intervention. Method of measurement: blood sample.;Leptin. Timepoint: before and after the intervention. Method of measurement: blood sample.;Nutritional status. Timepoint: before and after the intervention. Method of measurement: MIS.;IL-6. Timepoint: before and after the intervention. Method of measurement: blood sample.

Secondary

MeasureTime frame
Adverse drug reactions. Timepoint: during intervention. Method of measurement: patient-based reports.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Jamshid Roozbeh

Shiraz University of Medical Sciences, Nephrology Department

roozbehj@hotmail.com+98 71 3647 4316

Outcome results

None listed

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