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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04768751
Other study ID # Acute Kidney injury
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 5, 2019
Est. completion date August 30, 2020

Study information

Verified date February 2021
Source South Egypt Cancer Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute kidney injury (AKI) is classically described as an abrupt or rapidly reversible reduction in the excretion of nitrogenous waste products, including urea, nitrogen and creatinine. Acute kidney injury definition emphasizes on the filtration function of the kidney, a measure that is unique and easily and routinely measured . Acute kidney injury is associated with significantly increased resource utilization and health care costs. Major adverse cardiac events (MACE) after non cardiac surgery are a leading cause of morbidity and mortality. The reported incidence of postoperative myocardial infarction (POMI) among patients undergoing non cardiac surgery is between 3% and 6%.


Recruitment information / eligibility

Status Completed
Enrollment 520
Est. completion date August 30, 2020
Est. primary completion date August 20, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Patients with normal kidney functions and free normal heart functions, were enrolled to this study Exclusion Criteria: - patients with chronic kidney disease, cardiac disease, who with minor operations, or emergency, were excluded from the study.

Study Design


Intervention

Diagnostic Test:
kidney assessment
Urea, BUN, and Creatinine BLOOD LEVELS

Locations

Country Name City State
Egypt Alaa Ali Elzohry Assuit

Sponsors (1)

Lead Sponsor Collaborator
South Egypt Cancer Institute

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary development myocardial injury New echocardiographic findings suggestive of ischemia (new regional wall motion abnormalities) or cardiac troponin T >.0.32 ng/ml through study completion, an average of 15 days
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