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Effects of oral iron supplementation on the gut microbiome and plasma uremic toxin levels in patients with chronic kidney disease

Effects of oral iron supplementation on the gut microbiome and plasma uremic toxin levels in patients with chronic kidney disease - Effect of oral iron on gut-derived uremic toxin levels in CKD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON41855
Enrollment
10
Registered
2015-02-19
Start date
2015-11-18
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Iron deficiency in CKD

Interventions

None listed

Sponsors

Laboratoriumgeneeskunde
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18-80 years 2. CKD stage III-IV (GFR of 15-60 ml/min /1.73m2) 3. Iron deficient and an indication for treatment with ferrous fumarate, that is Hb

Exclusion criteria

Exclusion criteria: 1. Patients already under treatment with iron (orally or intravenously), or finished iron treatment

Design outcomes

Primary

MeasureTime frame
Blood uremic toxin levels (13 uremic toxins: hippurate, indoles (indoxyl sulfate, indoxyl glucuronide and indole-3-acetic acid, tryptophan metabolites (kynurenine, kynureninic acid and quinolinic acid), phenols (phenyl acetic acid, phenyl sulphate, phenyl glucuronide, 3-carboxy-4-methyl-5-propyl-2-furanpropionic acid (CMPF), p-cresyl sulfate and p-cresyl glucuronide), before, during, and after iron treatment.

Secondary

MeasureTime frame
• Faecal uremic toxin levels (13 uremic toxins; see above), before, during, and after iron treatment • Gut microbiome composition, before, during, and after iron treatment • Gut microbial proteolytic activity by faecal ammonia, before, during, and after iron treatment • Blood ammonia levels, before, during, and after iron treatment • Faecal iron content (for correlation with the gut microbiome composition) • Other blood parameters: Hb (hemoglobin), MCV (Mean Corpuscular Volume), Fe, TIBC (Total iron binding capacity), ferritin, CRP (C-reactive protein), creatinine (estimation GFR). o The transferrin saturation will be calculated based on TIBC and Fe.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)