Comparative study of the effect of oral liquid therapy with intravenous fluid therapy on the adequacy of renal function after Angiography and Angioplasty

Not Applicable

Conditions: Condition 1: angiography. Condition 2: Angioplasty.
Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Registration Number: IRCT20181122041722N1

Lead Sponsor: Sabzevar University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 120

Inclusion Criteria

Patients with EF more than 35%.
Creatinine is less than 1.5.
Patients who do not have ESRD and do not undergo dialysis.
Patients with stable hemodynamic status and blood pressure greater than 90mmHg.
The calculated GFR values are above 30 CC / min / 1.73.
Older people are 18 years of age and under 70 years of age.

Exclusion Criteria

People who have gastrointestinal illness after consulting a gastroenterologist
Patients with kidney problems
Patients taking medications that are effective in kidney function.

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Changes in creatinine before, after angiography, with an increase in cr content of more than 25% of baseline, or more than 0.5 mg / dl of creatinine increase, is considered as an incidence of CIN. Timepoint: Blood creatinine measurements at the beginning of the study (before the intervention) and 48 hours after the intervention. Method of measurement: The blood creatinine test carried out by the Bt4500 device.;Level Of GFR. Timepoint: Before Of Intervention And 48 hours after intervention. Method of measurement: Due to the formula * Cockcroft-Gault.;Level Of EF. Timepoint: Before Of Intervention. Method of measurement: With an electrocardiograph device.;Kidney function adequacy. Timepoint: 48 hours after intervention. Method of measurement: GFR evaluation.

Secondary Outcome Measures