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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03010735
Other study ID # CAUPCKD-02
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date June 2015
Est. completion date December 2017

Study information

Verified date October 2020
Source China Agricultural University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of oral administration of probiotics on the metabolism of uremic toxins, in the patients with End Stage Renal Disease (ESRD). One hundred and fifty hemodialysis patients are recruited, and a Double Blind Randomized Parallel Controlled Trial was performed.The microbiota-derived uremic toxin, such as indoxyl sulfate and p-cresol sulfate, are measured as Primary Outcome. The Fecal microbiome, fecal metabolites, blood metabolites, defecation, Gastrointestinal Symptoms The Kidney Disease Quality of Life and The Occurrence of Cardiovascular Event are also assessed.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date December 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age over 18 years old - Patients who diagnosed as ESRD with hemodialysis - Fixed hemodialysis cycle (average 3 times a week) - Agree to take the products to be studied during the study period, and no longer take other fermented dairy products (live lactic acid bacteria drinks, cheese, yogurt, probiotic products, etc.) - Agree to sign the informed consent form Exclusion Criteria: - Taking antibiotics or antifungal drugs within 30 days before the study - Have serious allergic reaction to skim milk powder - Researcher are not sure whether the subjects are willing or able to complete the study - Subject participated in other research projects within two months before the study

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
probiotics
Daily take 4.0E+10 CFU of probiotics
Placebo


Locations

Country Name City State
China Beijing Anzhen Hospital Beijing
China General Hospital of Chinese Armed Police Forces Beijing
China Peking University Aerospace Centre Hospital Beijing

Sponsors (6)

Lead Sponsor Collaborator
China Agricultural University Beijing Anzhen Hospital, Beijing Biostats Technology Co. Ltd., Beijing Heyiyuan Biotech Co. Ltd., General Hospital of Chinese Armed Police Forces, Peking University Aerospace Centre Hospital

Country where clinical trial is conducted

China, 

References & Publications (8)

Anders HJ, Andersen K, Stecher B. The intestinal microbiota, a leaky gut, and abnormal immunity in kidney disease. Kidney Int. 2013 Jun;83(6):1010-6. doi: 10.1038/ki.2012.440. Epub 2013 Jan 16. Review. — View Citation

Aronov PA, Luo FJ, Plummer NS, Quan Z, Holmes S, Hostetter TH, Meyer TW. Colonic contribution to uremic solutes. J Am Soc Nephrol. 2011 Sep;22(9):1769-76. doi: 10.1681/ASN.2010121220. Epub 2011 Jul 22. — View Citation

Koppe L, Mafra D, Fouque D. Probiotics and chronic kidney disease. Kidney Int. 2015 Nov;88(5):958-66. doi: 10.1038/ki.2015.255. Epub 2015 Sep 16. Review. — View Citation

Meyer TW, Hostetter TH. Uremia. N Engl J Med. 2007 Sep 27;357(13):1316-25. Review. — View Citation

Poesen R, Claes K, Evenepoel P, de Loor H, Augustijns P, Kuypers D, Meijers B. Microbiota-Derived Phenylacetylglutamine Associates with Overall Mortality and Cardiovascular Disease in Patients with CKD. J Am Soc Nephrol. 2016 Nov;27(11):3479-3487. Epub 2016 May 26. — View Citation

Poesen R, Windey K, Neven E, Kuypers D, De Preter V, Augustijns P, D'Haese P, Evenepoel P, Verbeke K, Meijers B. The Influence of CKD on Colonic Microbial Metabolism. J Am Soc Nephrol. 2016 May;27(5):1389-99. doi: 10.1681/ASN.2015030279. Epub 2015 Sep 23. — View Citation

Ramezani A, Raj DS. The gut microbiome, kidney disease, and targeted interventions. J Am Soc Nephrol. 2014 Apr;25(4):657-70. doi: 10.1681/ASN.2013080905. Epub 2013 Nov 14. Review. — View Citation

Vaziri ND, Wong J, Pahl M, Piceno YM, Yuan J, DeSantis TZ, Ni Z, Nguyen TH, Andersen GL. Chronic kidney disease alters intestinal microbial flora. Kidney Int. 2013 Feb;83(2):308-15. doi: 10.1038/ki.2012.345. Epub 2012 Sep 19. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Microbiota-derived uremic toxin follow up the patients at Month 0, 3, 6 6 months
Secondary Changes in Fecal Microbiome follow up the patients at Month 0, 3, 6 6 months
Secondary Changes in Fecal metabolites follow up the patients at Month 0, 3, 6 6 months
Secondary Changes in Blood metabolites follow up the patients at Month 0, 3, 6 6 months
Secondary Defecation questionnaire follow up the patients at Month 0, 3, 6 6 months
Secondary Gastrointestinal Symptoms follow up the patients at Month 0, 3, 6 6 months
Secondary The Kidney Disease Quality of Life follow up the patients at Month 0, 3, 6 6 months
Secondary The Occurrence of Cardiovascular Event 6 month follow-up
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