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Prevention of Perioperative Acute Renal Failure

NCT00953940 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2011-07-04

No results posted yet for this study

Summary

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

Conditions

  • Abdominal Surgery

Interventions

DRUG

Isotonic saline

Isotonic saline administrated i.v at 1.5 ml/Kg/h , 8 to 12 h before surgery

Sponsors & Collaborators

  • Fondo de Investigacion Sanitaria

    collaborator OTHER

  • Hospital Universitario Ramon y Cajal

    lead OTHER

Principal Investigators

  • Dr Fernando Liaño, MD PhD · Hospital Universitario Ramon y Cajal

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2011-02-28
Completion
2011-05-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00953940 on ClinicalTrials.gov