Prevention of Perioperative Acute Renal Failure

Phase 4

Terminated

• Conditions: Abdominal Surgery
• Interventions: Drug: Isotonic saline

• Registration Number: NCT00953940
• Lead Sponsor: Hospital Universitario Ramon y Cajal

Brief Summary

The purpose of this study is to measure the acute renal dysfunction on the first, second, seventh and twentieth days.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-06
• Status Verified: 2009-08
• Study First Submitted: 2009-08-04
• Study First Submitted QC: 2009-08-05
• Study First Posted: 2009-08-06
• Primary Completion: 2011-02
• Study Completion: 2011-05
• Last Update Submitted: 2011-06-30
• Last Update Posted: 2011-07-04

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 600

Inclusion Criteria

• 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 Criteria

• 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Isotonic saline	Isotonic saline	Isotonic saline

Primary Outcome Measures

Name	Time	Method
Serum creatinine in the first, second, seventh and twenty after surgery in patients undergoing elective abdominal surgery.	5 years

Trial Locations

Locations (1)

Hospital Ramon y Cajal; 🇪🇸 Madrid, Spain