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NCT00310739 Clinical Trial

Urinary Marker for Oxidative Stress in Human Cisplatin- Induced Renal Injury

Kidney Failure Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00310739
Other study ID # 16-50
Secondary ID
Status Recruiting
Phase N/A
First received April 3, 2006
Last updated November 6, 2006

Study information
Verified date April 2005
Source Hamamatsu University
Contact Takayuki Tsuji, MD
Phone +81-53-435-2261
Email tsu@hama-med.ac.jp
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational

Clinical Trial Summary

We previously reported early measurement of urinary MDA might be a useful marker for the prediction of CDDP-induced renal damage in rat. The purpose of this clinical study is to test whether the changes of human urinary excretion of MDA, and can be used as early biomarker for the prediction of development of CDDP-induced ARF.

Recruitment information / eligibility
Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Hospitalized patients have neck cancer

Study Design

Observational Model: Natural History, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Locations
Country Name City State
Japan Hamamatsu University School of Medicine Hamamatsu Shizuoka

Sponsors (1)
Lead Sponsor Collaborator
Hamamatsu University

Country where clinical trial is conducted

Japan, 

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