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Effect of personalized micronutrient supplementation among severe acute kidney injury patients undergoing renal replacement therapy : a randomized controlled trial

Effect of personalized micronutrient supplementation among severe acute kidney injury patients undergoing renal replacement therapy : a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260324001
Enrollment
46
Registered
2026-03-24
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Severe acute kidney injury (KDIGO stage 3) in critically ill patients undergoing renal replacement therapy (CRRT or SLED) Critical illness acute kidney injury Renal replacement therapy Micronutrient supplementation SOFA score

Interventions

Participants in the intervention group will receive personalized micronutrient supplementation based on plasma levels of vitamin C, zinc, and selenium. Supplementation will be provided when deficiency
Experimental Dietary Supplement,No Intervention No treatment
micronutrient supplementation ,Standard of care

Sponsors

Faculty of Medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1.Age more than 18 years 2.ICU patients with severe acute kidney injury KDIGO stage 3 3.Receiving renal replacement therapy CRRT or SLED 4. Informed consent obtained from patient or legal representative

Exclusion criteria

Exclusion criteria: 1.Use of oral nutritional supplements 2. ICU stay more than 7 days before enrollment 3. Receiving parenteral nutrition 4. History of kidney transplantation 5.Pregnancy or breastfeeding 6.Known allergy to study supplements 7.Acute liver failure or fulminant hepatitis

Design outcomes

Primary

MeasureTime frame
Change in Sequential Organ Failure Assessment-2 (SOFA-2) score 28 day Sequential Organ Failure Assessment-2 (SOFA-2) score calculated using clinical and laboratory parameters.

Secondary

MeasureTime frame
Duration of renal replacement therapy 28 days Number of days receiving renal replacement therapy recorded from medical records.,Length of ICU stay 28 days Number of days receiving renal replacement therapy recorded from medical records,Duration of mechanical ventilation 28 days Number of days receiving mechanical ventilation from initiation to discontinuation, obtained from medical records.,C-reactive protein (CRP) level 28 days Serum CRP level measured using standard laboratory assay from blood samples.,Interleukin-6 (IL-6) level 28 days Serum Interleukin-6 (IL-6) level measured using standard laboratory assay from blood samples.,Total antioxidant capacity 28 days Total antioxidant capacity measured using standard laboratory assay from blood samples.

Countries

Thailand

Contacts

Public ContactBhurapol Prommongkol

Nephrology department King Chulalongkorn Memorial Hospital

bhpr.med@gmail.com0953545144

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026