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Study of Urinary Angiotensinogen as a Marker to Warn the Deterioration of Renal Function in CKD Patients Early.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01118494
Enrollment
400
Registered
2010-05-06
Start date
2009-09-30
Completion date
2011-06-30
Last updated
2010-05-06

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

Conditions

Chronic Kidney Disease, Urinary Angiotensinogen

Keywords

CKD, RAS, AGT

Brief summary

Chronic kidney disease (CKD) that results in end-stage renal disease (ESRD) is a major international health problem. Many clinical markers such as urine protein or eGFR(evaluated glomerular filtration rate),can estimate the renal function, but not sensitive. As well-known, the crucial role of angiotensin II (AngII), the major effector of the renin-angiotensin system (RAS), in the development of renal fibrosis that results in ESRD is widely recognized.Abundant researches find that intrarenal RAS takes an important role on the progression of CKD. At present, no clinical marker is available to evaluate intrarenal AngII activity because it is difficult to measure it directly in patients. So find and establish a bio-marker of local renal RAS activation maybe a breakthrough in early detection and treatment of CKD. Angiotensinogen(AGT) is the only known substrate for renin and the level of AGT in humans is close to Km value for renin. Thus , changes in AGT levels can control the activity of the RAS, and its up-regulation may lead to activity of Ang levels. Then we hypothesis that the AGT is a early bio-marker of local renal RAS activation as well as CKD.

Detailed description

1. Screening: Select CKD(3-4) patients from outpatients, Urine routine examination and Renal B-mode ultrasonography and so on. 2. Confirm: Sign consent with the patients who meet the inclusion criteria, then these patients are included in the study. 3. Create patients records and complete related-inspections. 4. Clinical follow-up: Follow-up once every six months, and we will record every patient's disease progress every time. Each follow-up, the patient needs to leave 5 ml blood samples and 20 ml of urine samples, used for the following study. 5. Detection, Observation and Evaluation: Patients are divided into two groups according to AGT levels: higher than the normal group and the normal group. Observe the changes in eGFR of different group. Statistics judge whether AGT can be as a early warning indicators of renal function decline.

Interventions

None listed

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* CKD, in the stage of 3 or 4, and kidney biopsy is preferred selection; * Signed the informed consent;

Exclusion criteria

* Kidney cancer patients; * Kidney transplantation; * Hereditary kidney disease; * Secondary renal disease(diabetic nephropathy and hypertensive nephropathy are excluded)

Design outcomes

Primary

MeasureTime frameDescription
Urinary AGT level12 monthsUrinary AGT level can be an early bio-marker of intrarenal RAS activation and prewarning the deterioration of renal function.

Countries

China

Contacts

Primary ContactYong Gu, doctor
yonggu@vip.163.com13916322128

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026