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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06146829
Other study ID # TJH-20230608C
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 27, 2023
Est. completion date December 15, 2023

Study information

Verified date April 2024
Source Tongji Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute kidney injury (AKI) is a common surgical complication characterized by a rapid decline in renal function. Patients with AKI are at an increased risk of developing chronic kidney disease and end-stage renal disease, which has been associated with an increased risk of morbidity, mortality and financial burdens. Identifying high-risk patients for postoperative AKI early can facilitate the development of preventive and therapeutic management strategies, and prediction models can be helpful in this regard. The goal of this retrospective study is to develop prediction models for postoperative AKI in noncardiac surgery using machine learning algorithms, and to simplify the models by including only preoperative variables or only important predictors.


Recruitment information / eligibility

Status Completed
Enrollment 88367
Est. completion date December 15, 2023
Est. primary completion date December 15, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients (age = 18 years) who had a serum creatinine measurement within 10 days before surgery and at least one measurement within 7 days after surgery. - Eligible surgeries encompassed general, thoracic, orthopedic, obstetric, gynecology, and neurosurgery procedures lasting longer than 1 hour Exclusion Criteria: - Patients with concurrent cardiac, vascular, urological, or transplant surgeries. - Patients with an American Society of Anesthesiologists (ASA) physical status V. - Patients with end-stage renal disease (i.e., a glomerular filtration rate [eGFR] of 15 mL/min/1.73 m² or receiving hemodialysis).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
no intervention
no intervention

Locations

Country Name City State
China Rao Sun Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Rao Sun

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative acute kidney injury In accordance with the KDIGO creatinine criteria: a serum creatinine increases of 26.5 mmol/L within 48 hours or 1.5 times baseline within 7 days after surgery. Within 7 days after surgery
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