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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03954353
Other study ID # ECAKI
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 17, 2019
Est. completion date June 6, 2019

Study information

Verified date July 2019
Source Peking University First Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Preoperative serum cholesterol level may influence occurrence of postoperative acute kidney injury of cardiac surgeries. However, the effect of Preoperative serum cholesterol level for non cardiac surgery remains unknown. This study aimed to explore the effect in non-cardiac surgical population.


Recruitment information / eligibility

Status Completed
Enrollment 78888
Est. completion date June 6, 2019
Est. primary completion date June 5, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

adults elective non-cardiac surgery

Exclusion Criteria:

cardiac surgeries kidney surgeries obstetric surgeries local infiltration anesthesia perioperative data missing

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China First hospital Peking University Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University First Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary post-operative acute kidney injury within 30 days in the hospital It was defined by patient's postoperative serum creatine increase no less than 26.5 µmol/l within 48 hours, or 1.5 times from baseline within the 7 days after surgery or initializing blood dialysis. 30 days postoperatively in hospital
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