Clinical Trials Directory

Trials / Completed

CompletedNCT02137863

Efficacy of Dexmedetomidine in Preventing Contrast Induced Nephropathy

Phase 4 Study of Dexmedetomidine Effects on Preventing Contrast Induced Nephropathy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
TC Erciyes University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study was to evaluate the effects of dexmedetomidine on renal function, hormonal and hemodynamic parameters in contrast media induced diabetic patients.

Detailed description

Contrast nephropathy may occur after using intravenous contrast media and may result in acute renal failure. Contrast nephropathy usually reversible but in some cases it can be permanent. This situation increase the time of hospitalization and mortality of the patients. Although the only proved prevention from contrast nephropathy method is hydration, infusion of dexmedetomidine may keep the renal functions.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineIntravenously 1μg/kg/10min administered just before the procedure. 1 μg/kg/h administered during the angiography and was continued 1 hour after the angiography.
DRUG0.9 % NaClDuring 12 hours before the procedure 3 ml/kg/h 0.9 % NaCl infusion and 1 ml/kg/h during the angioplasty and 12 hours after the procedure.
DRUG0.9 % NaCl100 ml/10min infusion just before the angiography 1 ml/kg/h infusion during the angiography and was continued 12 hours after the procedure

Timeline

Start date
2011-06-01
Primary completion
2012-06-01
Completion
2012-07-01
First posted
2014-05-14
Last updated
2014-05-14

Source: ClinicalTrials.gov record NCT02137863. Inclusion in this directory is not an endorsement.