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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01752738
Other study ID # S54909
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 2013
Est. completion date December 31, 2022

Study information

Verified date April 2020
Source Universitaire Ziekenhuizen Leuven
Contact Sander Derjongh
Phone + 32 16 342352
Email sander.dejongh@kuleuven.be
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chronic kidney disease is associated with the accumulation of various metabolites, i.e., uremic retention solutes. Evidence is mounting that the colonic microbiome contributes substantially to these uremic retention solutes. Indoxyl sulfate and p-cresyl sulfate are among the most extensively studied gut microbial metabolites, and are associated with cardiovascular disease, chronic kidney disease progression and overall mortality. Mechanisms governing their intestinal uptake and metabolism, however, are currently unknown. The investigators aim to explore these transport characteristics in depth. Therefore, colonic biopsies will be sampled of patients with chronic kidney disease, analyzed and compared to available data of healthy controls. Insights in the mechanisms controlling intestinal transport and metabolism of indoxyl sulfate and p-cresyl sulfate is certainly relevant as it might lead to novel therapeutic targets in the treatment of chronic kidney disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Age = 18 and = 85 years

- Chronic kidney disease = stage III (KDOQI), i.e., estimated glomerular filtration rate (MDRD) < 60 ml/min/m² or need of dialysis therapy 27

- Scheduled colonoscopy for diagnostic purposes

- Written informed consent

Exclusion Criteria:

- History of gastro-intestinal disease (e.g., inflammatory bowel disease)

- History of colon surgery

- Recipient of a renal or other solid organ transplant

- Exposure to antibiotics or drug therapy with a known influence on intestinal transporters (e.g., P-gp) or enzymes during 2 weeks before colonoscopy

Study Design


Locations

Country Name City State
Belgium University Hospitals Leuven Leuven Vlaams Brabant

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage change in number of intestinal drug transporters and enzymes Influence of chronic kidney disease on intestinal drug transporters and enzymes responsible for uptake and metabolism of microbial metabolites 4 years
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