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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00158080
Other study ID # K0001
Secondary ID
Status Recruiting
Phase N/A
First received September 7, 2005
Last updated September 7, 2005

Study information

Verified date September 2005
Source Nara Medical University
Contact Koji Harada, MD
Phone +81-744-22-3051
Email kzharada@naramed-u.ac.jp
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

Contrast-induced acute renal failure can be prevented with hemofiltration which is performed during cardiac catheterization


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients with serum creatinine>2.0mg/dl and/or GFR<50ml/min

Exclusion Criteria:

- Emergent cardiac catheterization

- Patients on chronic dialysis

- Patients with HYHA>III heart failure

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Procedure:
hemofiltration


Locations

Country Name City State
Japan First Dept of InternalMedicine, Nara Medical University Kashihara Nara

Sponsors (1)

Lead Sponsor Collaborator
Nara Medical University

Country where clinical trial is conducted

Japan, 

References & Publications (1)

Kashyap AS, Anand KP, Kashyap S. Hemofiltration and the prevention of radiocontrast-agent-induced nephropathy. N Engl J Med. 2004 Feb 19;350(8):836-8; author reply 836-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Prevention of contrast-induced acute renal failure, Elevation of serum creatinine
Secondary Need for hemodialysis
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