Status:
TERMINATED
Prevention of Perioperative Acute Renal Failure
Lead Sponsor:
Hospital Universitario Ramon y Cajal
Collaborating Sponsors:
Fondo de Investigacion Sanitaria
Conditions:
Abdominal Surgery
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to measure the acute renal dysfunction on the first, second, seventh and twentieth days.
Eligibility Criteria
Inclusion
- All patients who are undergoing elective abdominal surgery after appropriate information of the study, and its possible risks that may arise therefrom and that at any time to refuse their cooperation, give a written consent to participate in the study.
- Patients who at the time of the interview have an ASA between 2 and 4.
- Patients with chronic kidney failure mild moderate (serum creatinine between 1.5 and 3.0 mg / dl) can be included.
Exclusion
- Chronic kidney diseases with serum creatinine higher than 3.0 mg /DL
- Laparoscopic abdominal surgery
- ASA 1 and ASA 5 patients.
- Patients with cardiac insufficiency, ascites and respiratory insufficiency
- Diastolic hypertension \> 100 mmHg
Key Trial Info
Start Date :
June 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2011
Estimated Enrollment :
600 Patients enrolled
Trial Details
Trial ID
NCT00953940
Start Date
June 1 2005
End Date
May 1 2011
Last Update
July 4 2011
Active Locations (1)
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1
Hospital Ramon y Cajal
Madrid, Madrid, Spain, 28034