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Role of pharmacist in End-Stage Renal Disease

EFFECT OF SYNBIOTICS ON SERUM UREMIC TOXINS LEVEL IN END STAGE RENAL DISEASE PATIENTS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058396
Enrollment
35
Registered
2023-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: N186- End stage renal disease

Interventions

Intervention1: SYNBIOTICS: Intervention which include prescribing pro/pre-biotics and providing with dietary modifications(decreased protein intake and increased fiber intake) will be undertaken. The

Sponsors

College of Pharmacy,SRIPMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient undergoing hemodialysis and patient signing patient consent form.

Exclusion criteria

Exclusion criteria: Patient who have previously failed renal transplantation , who have ESRD of inflammatory cause(lupus, vasculitis, collagenopathies) , who had intake of probiotics,prebiotics in last 3 months, who have any medical condition affecting intestinal absorption(inflammatory bowel disease,short bowel syndrome, bariatric surgery) or severe dysmotility, who are taking any alternative medicine other than allopathic medicine, who are frail , who are treated with antibiotics , with severe malnutrition and with severe other diseases.

Design outcomes

Primary

MeasureTime frame
Change of uremic toxin from baseline to 6th week and 12th week. Measurement of serum concentrations of the uremic toxin indoxyl sulphate (mg/dL) by means of HPLC technique.Timepoint: Change of uremic toxin from baseline to 6th week and 12th week. Measurement of serum concentrations of the uremic toxin indoxyl sulphate (mg/dL) by means of HPLC technique.

Secondary

MeasureTime frame
Change in gastrointestinal symptoms from baseline to 3rd and 6th month. Measurement of appetite and frequency and severity of gastrointestinal symptoms(nausea,vomiting,bloating,diarrhea,constipation)by means of GSRS questionnaire. Change in serum creatinine level and eGFR rate from baseline to 3rd and 6th monthTimepoint: baseline , 3rd ,6th month

Countries

India

Contacts

Public ContactMs S Madhu mitha

College of pharmacy,SRIPMS

mail2samjohnson@gmail.com9894676716

Outcome results

None listed

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