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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02838667
Other study ID # 16-003845
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2016
Est. completion date June 10, 2019

Study information

Verified date October 2019
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nephrology participation in care of patients undergoing CABG could reduce AKI through correction of modifiable risk factors and early detection and intervention of post-op AKI.


Recruitment information / eligibility

Status Completed
Enrollment 2300
Est. completion date June 10, 2019
Est. primary completion date June 10, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients (Age >18 years)

- Elective CABG at Mayo Clinic Rochester and Shanghai Zhongshan Hospital from 7/1/2016 to 6/30/2017

Exclusion Criteria:

- Non-elective CABG

- Renal failure on dialysis

- Renal transplantation

Study Design


Intervention

Procedure:
Standard of Care plus Nephrology Care


Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perfusion pressures (mean arterial pressure) = 65-70 mmHg baseline to 5 days
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