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A STUDY OF PROGNOSTOIC SIGNIFICANCE OF PRE â?? PROCEDURAL RENAL RESISTIVE INDEX (RI) FOR THE PREDICTION OF CONTRAST INDUCED ACUTE KIDNEY INJURY IN PATIENTS WITH CORONARY ARTERY DISEASE (CAD) WITH PRESERVED RENAL FUNCTION UNDERGOING ELECTIVE CORONARY ANGIOGRAPHY.

Not Applicable
Conditions
Health Condition 1: I213- ST elevation (STEMI) myocardial infarction of unspecified site
Registration Number
CTRI/2023/04/051294
Lead Sponsor
DR SATYASISH KABI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patientswithstableanginawithpositivetreadmilltest

2. Patients with ST elevation acute coronary syndrome after thrombolysis

3. Patients with Non ST elevation acute coronary syndrome

4. PatientswithUnstableangina

Exclusion Criteria

1. Significant hemodynamic instability (cardiogenic shock; killip class >2;

catecholamine use)

2. Respiratory failure (acute or chronic; blood oxygen saturation <90%)

3. Severe heart failure with left ventricular ejection fraction (LVEF <35%)

4. Chronic kidney disease (with eGFR < 50 mL/min/1.73 m2 or proteinuria

>500 mg/L)

5. Evidence of renal artery stenosis or hydronephrosis

6. Moderate to severe aortic valve stenosis

7. Severe valvular heart disease of any kind

8. Severe obesity (body mass index, BMI > 40 kg/m2)

9. Liver dysfunction (any hepatic aminotransferase >3Ã? upper reference

limit)

10. Age <18 or >80 years old

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate significance of pre-operative ultrasonographic parameter of intra renal blood flow (RRI), for prediction of contrast induced acute kidney injury in patients with coronary artery disease and preserved renal function, referred for elective coronary angiography.Timepoint: 52 week
Secondary Outcome Measures
NameTimeMethod
To suggest the possible application of renal resistive index (RRI) during initial check up of patient along with other routine investigation for risk stratification of patients, prone for contrast induced acute kidney injury.Timepoint: 52 weeks
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