Effects of BRS and LRS on Postoperative Acute Kidney Injury
Last updated on July 2021Recruitment
- Recruitment Status
- Not yet recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Acute Kidney Injury
- Type
- Interventional
- Phase
- Phase 4
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Other
Participation Requirements
- Age
- Between 20 years and 70 years
- Gender
- Both males and females
Description
Subjects: patients who planned to undergo elective major abdominal surgery. Study data collection period: Subjects signed the consent form until 28 days after discharge or died in hospital or withdrew from the study. Number of research centers/sample size: 3400 patients were planned to be included. ...
Subjects: patients who planned to undergo elective major abdominal surgery. Study data collection period: Subjects signed the consent form until 28 days after discharge or died in hospital or withdrew from the study. Number of research centers/sample size: 3400 patients were planned to be included. Study process: Among patients undergoing elective surgery, the researchers will include patients who meet the inclusion criteria for elective major abdominal surgery and agree to participate in the study. The data to be collected in this study will be recorded by the researcher in the eCRF, including: (1) Data to be collected during the screening period and preoperatively: patients' basic characteristics and demographic data (2) Data to be recorded during and/or after surgery: primary study indicators, secondary indicators, and other indicators.
Tracking Information
- NCT #
- NCT04835038
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Shiyong Li Tongji Hospital
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