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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00467311
Date of registration: 27/04/2007
Primary sponsor: National Heart Institute, Mexico
Public title: Cystatin C as an Early Marker of Contrast-Medium Nephropathy in Cardiac Catheterization Patients
Scientific title: Diagnostic, Transversal, Comparative, Not Randomized Trial for the Evaluation of Cystatin C as an Early Marker of Contrast-Medium Nephropathy in High-and-Intermedium-Risk Patients Undergoing to Cardiac Catheterization
Date of first enrolment: December 2006
Target sample size: 66
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00467311
Study type:  Observational
Study design:  Time Perspective: Cross-Sectional  
Countries of recruitment
Mexico
Contacts
Name:   Jhonathan L Uribe-González, MD, MSc
Address: 
Telephone:
Email:
Affiliation:  Ignacio Chávez National Institute of Cardiology
Name:   Jorge G Hernández, MD, FSCAI
Address: 
Telephone:
Email:
Affiliation:  Ignacio Chávez National Institute of Cardiology
Name:   Marco A Martínez-Rios
Address: 
Telephone:
Email:
Affiliation:  Ignacio Chávez National Institute of Cardiology
Name:   Marco A Peña-Duque, MD
Address: 
Telephone:
Email:
Affiliation:  Ignacio Chávez National Institute of Cardiology
Key inclusion & exclusion criteria

Inclusion Criteria:

- Age over 20 years old

- Indication for coronariography and/or percutaneous coronary intervention

- Voluntary written consent for the realization of coronariography and/or percutaneous
intervention and for the participation in this clinical trial

- A MEHRAN contrast-induced nephropathy score from six to fifteen.

Exclusion Criteria:

- N-Acetylcystein and Fenoldopam pre-medication

- Low risk patients according MEHRAN classification

- Cardiogenic and septic shock

- Acute renal failure by any other cause

- Patients with chronic kidney failure requiring any kind of dialysis

- Patients unable to complete follow-up

- Exposure to contrast media 48 hours prior to study

- Patients unable to give consent

- Receiving contrast media other than non-ionic



Age minimum: 20 Years
Age maximum: 85 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Acute Renal Failure
Contrast Induced Nephropathy
Intervention(s)
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
07552
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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