This study evaluates if oral hydratation is as effective as endovenous hydratation in the
prophylaxis of contrast-induced nephropathy in patients renal insufficiency grade III under
study conducting contrasted computed tomography.
Other: Oral hydratation
Drug: Bicarbonate endovenous hydratation
Drug: Saline endovenous hydratation
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Locations near you
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Full eligibility criteria for NCT02872155
Ages eligible for Study
18 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
- Patients of both sexes over 18 years
- Candidates for a study with computed tomography and intravenous contrast
- A glomerular filtration rate between 30 and 45 mL / min including both determinations
- They have signed the written informed consent after being informed of the objectives
and the nature of the case or be unable to have the authorization or agreement of its
- refuse to participate in the study
- pregnancy or lactation
- Other risk factors for Contrast Induced Nephropathy: diabetes mellitus type I, have an
age of 75 years or above, heart failure (defined by a scale New York Heart Association
3 or 4), hypotension (defined as systolic blood pressure <100), being treated with
- Any disease or a history that, in the investigator's opinion, could confound the
results of the study or pose an additional risk to patient treatment.
All locations for NCT02872155
Barcelona, Spain, 08003
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View full eligibility
Tris trial is registered with FDA with number: NCT02872155. The sponsor of the trial is David Garcia Cinca and it is looking for 264 volunteers for the current phase.
Official trial title: Comparative Study of the Efficacy of Oral Versus Intravenous Hydration as a Preventive Measure of Contrast-induced Nephropathy (CIN) in Patients
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