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Perioperative Mechanism of Acute Kidney Injury in Cardiovascular Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03557047
Recruitment Status : Unknown
Verified March 2018 by The First Affiliated Hospital of Anhui Medical University.
Recruitment status was:  Recruiting
First Posted : June 14, 2018
Last Update Posted : July 3, 2018
Sponsor:
Information provided by (Responsible Party):
The First Affiliated Hospital of Anhui Medical University

Study Description
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Brief Summary:
Continuous observation of acute renal injury after cardiac surgery, at the same time retention of blood samples, to test indicators，and to select the research route from the clinical actual test results .

Condition or disease
Pathogenesis Acute Kidney Injury Cardiac Surgery

Study Design
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Study Type : Observational [Patient Registry]
Estimated Enrollment : 50 participants
Observational Model: Other
Time Perspective: Prospective
Target Follow-Up Duration: 1 Week
Official Title: Preliminary Study on the Pathogenesis of Acute Kidney Injury After Cardiac Surgery
Actual Study Start Date : March 8, 2018
Estimated Primary Completion Date : March 2021
Estimated Study Completion Date : September 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Surgery

Groups and Cohorts
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Outcome Measures
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Primary Outcome Measures :
  1. Incidence of acute renal injury after cardiac surgery [ Time Frame: 48 hours ]
    The standard of acute renal injury is based on the KDIGO


Eligibility Criteria
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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Perioperative data were collected, including cardiopulmonary bypass time，aortic cross-clamping time, operative time, extubation time, ICU time and hospital stay.
Criteria

Inclusion Criteria:

  • Adult patients undergoing selective cardiac surgery, aged between 18 and 80.

Exclusion Criteria:

  • Normal range of creatinine before operation
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03557047


Locations
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China, Anhui
The First Affiliated Hospital of Anhui Medical University Recruiting
Hefei, Anhui, China, 230022
Contact: Qian Gong    (086)13485690649    54xiaoqian@sina.com   
Sponsors and Collaborators
The First Affiliated Hospital of Anhui Medical University
More Information
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Additional Information:

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Responsible Party: The First Affiliated Hospital of Anhui Medical University
ClinicalTrials.gov Identifier: NCT03557047    
Other Study ID Numbers: PJ2018-03-10
First Posted: June 14, 2018    Key Record Dates
Last Update Posted: July 3, 2018
Last Verified: March 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Acute Kidney Injury
Wounds and Injuries
Renal Insufficiency
Kidney Diseases
Urologic Diseases