Effect of Cholesterol Level on Postoperative Acute Kidney Injury of Non-cardiac Surgeries
Sponsor
Peking University First Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03954353
Collaborator
(none)
78,888
1
20
120057.7
Study Details
Study Description
Brief 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.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
78888 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Effect of Cholesterol Level on Postoperative Acute Kidney Injury of Non-cardiac Surgeries
Actual Study Start Date
:
May 17, 2019
Actual Primary Completion Date
:
Jun 5, 2019
Actual Study Completion Date
:
Jun 6, 2019
Outcome Measures
Primary Outcome Measures
- post-operative acute kidney injury within 30 days in the hospital [30 days postoperatively in 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.
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
adults elective non-cardiac surgery
Exclusion Criteria:
cardiac surgeries kidney surgeries obstetric surgeries local infiltration anesthesia perioperative data missing
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | First hospital Peking University | Beijing | Beijing | China | 100034 |
Sponsors and Collaborators
- Peking University First Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Yan Zhou, MD,
Principal Investigator,
Peking University First Hospital
ClinicalTrials.gov Identifier:
NCT03954353
Other Study ID Numbers:
- ECAKI
First Posted:
May 17, 2019
Last Update Posted:
Jul 9, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: