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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03711617
Other study ID # CKD-toxins
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 1, 2018
Est. completion date December 31, 2024

Study information

Verified date November 2023
Source Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Contact Feng Ding, PhD
Phone 86-21-53315165
Email dingfeng@sjtu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this cohort study is: To investigate the etiology and epidemiology of comorbidities in CKD; To find out risk factors associated with the mortality of CKD; To find out uremic toxins which are related to the mortality and comorbidities of CKD; To focuse on the association between uremic toxins and inflammation, oxidative stress and nutritional status in CKD.


Description:

To investigate the etiology and epidemiology of comorbidities in CKD; To find out risk factors associated with the mortality of CKD; To find out uremic toxins which are related to the mortality and comorbidities of CKD; To focuse on the association between uremic toxins and inflammation, oxidative stress and nutritional status in CKD.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age =18 years old; - clinically diagnosed with chronic kidney disease, according K/DOQI criteria. Exclusion Criteria: - acute kidney injury - history of kidney injury <3 months - malignancy - pregnancy - incomplete clinical data

Study Design


Locations

Country Name City State
China Shanghai Ninth People's Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary all cause mortality 5 years
Secondary comorbidities 5 years
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