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The comparison of different types of fluid therapy in prevention of contrast induced renal malfunction in coronary angiography

Not Applicable
Conditions
contrast induced nephropathy.
Nephropathy induced by other drugs, medicaments and biological substances
Registration Number
IRCT2015080323483N1
Lead Sponsor
vice chancellor for research, Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
300
Inclusion Criteria

patients over 18 y/o who have indications for coronary angiography and angioplasty are included. However, patients with hemodynamic instability, severe cardiac failure or pulmonary edema, under dialysis, under medications potentially affecting kidney function or with electrolyte and acid-base disturbances are not included.
Exclusion criteria: patients with undesired complications such as arterial dissection during angiography or angioplasty are excluded from the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Creatinine. Timepoint: before and 48 hours after intervention. Method of measurement: Jaffe with adsorbent (picrate) method.;BUN. Timepoint: before and 48 hours after intervention. Method of measurement: urease/GLDH method.;Urine PH. Timepoint: before and 6 hours after intervention. Method of measurement: PH meter sticks.;Estimated GFR (eGFR). Timepoint: before and 48 hours after intervention. Method of measurement: MDRD equation.
Secondary Outcome Measures
NameTimeMethod
Sodium and Potassium (Na and K). Timepoint: before and 48 hours after intervention. Method of measurement: flame photometry method.
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