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Effect of synbiotic on severity uremic pruritus and muscle cramps in patients undergoing hemodialysis

Effect of synbiotic on severity uremic pruritus and muscle cramps in patients undergoing hemodialysis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250117064406N2
Enrollment
30
Registered
2025-12-19
Start date
2026-01-30
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Hemodialysis. Chronic kidney disease (CKD)

Interventions

Intervention 1: Intervention group: The intervention group will consume two synbiotic capsules with the brand name Lactocare (500 mg) daily, one after lunch and the other after dinner, for eight weeks

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Consent and interest in participating in the study Age 18 - 65 years old Hemodialysis treatment at least twice a week for a maximum of four hours each time Undergoing hemodialysis treatment for at least six months Presence of uremic pruritus as diagnosed by a doctor for at least six months and obtaining a score of at least mild on the YOSIPOVITCH questionnaire Experiencing muscle cramps at least once a week Life expectancy and survival for at least three months

Exclusion criteria

Exclusion criteria: Kidney and organ transplant candidates Consuming synbiotics, probiotics, prebiotics, or antibiotics four weeks before participating in the study Having a severe infection within four weeks before study participation Chronic liver disease (hepatitis B, hepatitis C), pulmonary, cardiovascular, acute pancreatitis, gastrointestinal disorders (inflammatory bowel disease, ulcerative colitis, Crohn's, celiac disease, lactose intolerance or allergy, irritable bowel syndrome), active cancers, immunodeficiency, HIV

Design outcomes

Primary

MeasureTime frame
Uremic pruritus severity. Timepoint: The severity of uremic pruritus will be measured before and after the intervention. Method of measurement: YOSIPOVITCH Itch Questionnaire.

Secondary

MeasureTime frame
Muscle cramps. Timepoint: Muscle cramps will be measured before and after the intervention. Method of measurement: Visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahein Momenabadi

Semnan University of Medical Sciences

shahein_momenabadi@yahoo.com+98 23 3344 1022

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026