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Clinical Trials/NCT00905775
NCT00905775
Terminated
Not Applicable

Evaluation of Renal Function and Oxidative Stress in Patients Submitted to Myocardial Revascularization Surgery, With Extracorporeal Circulation, and Anesthesia With Isoflurane or Propofol

UPECLIN HC FM Botucatu Unesp2 sites in 1 country60 target enrollmentDecember 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Disease
Sponsor
UPECLIN HC FM Botucatu Unesp
Enrollment
60
Locations
2
Status
Terminated
Last Updated
10 years ago

Overview

Brief Summary

Acute renal insufficiency (ARI) represents a frequent and serious complication in patients submitted to cardiac surgery, and is associated with increases in time of hospitalization, costs, morbidity and mortality. Its incidence varies from 3.5% to 31%. The present study aims to evaluate renal function and oxidative stress in patients submitted to revascularization surgery with extracorporeal circulation (ECC), comparing targeted venous anesthesia controlled with propofol and inhalational anesthesia with isoflurane.

Detailed Description

Acute renal insufficiency (ARI) represents a frequent and serious complication in patients submitted to cardiac surgery, and is associated with increases in time of hospitalization, costs, morbidity and mortality. Its incidence varies from 3.5% to 31%. The present study aims to evaluate renal function and oxidative stress in patients submitted to revascularization surgery with ECC, comparing targeted venous anesthesia controlled with propofol and inhalational anesthesia with isoflurane.The study will be conducted at the Botucatu Medical School (FMB) and will analyze 60 patients, divided into two randomized groups, submitted to revascularization surgery of the myocardium with ECC. The researcher responsible for data collection from patients will not have knowledge of the type of anesthesia being delivered to the patient.Blood samples will be collected by central venous access for dosing of troponin I, troponin T, CKMB, MDA, creatinine, urea, albumin and cystatin C.Renal function will be evaluated by serum cystatin C and creatinine and the estimated glomerular filtration rate (GFR). GFR will be measured by means of serum cystatin C (Larsson's formula) and by serum creatinine through the Cockcroft-Gault formula (CG) and by the MDRD formula (Modification of Diet in Renal Disease).Markers of renal tubular function will be dosed in the urine, including: alkaline phosphatase, γ - glutamyltransferase(γ-GT), β 2 microglobulin, creatinine and urinary cystatin C.

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
June 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
UPECLIN HC FM Botucatu Unesp
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • both sexes,
  • aged from 18 to 75 years,
  • submitted to revascularization surgery of the myocardium
  • extracorporeal circulation,
  • who had consented to participation by signing the Terms of Free and Clear Consent.

Exclusion Criteria

  • history of hepatic or renal dysfunction,
  • history involving acute myocardial infarct
  • patients that made use of vitamin C and E;
  • patients presenting other cardiac pathologies (valvular, congenital, corrected or not in the same operational act).

Outcomes

Primary Outcomes

Not specified

Study Sites (2)

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