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NCT06296108 Clinical Trial

Risk Factors for Acute Kidney Injury in Patients Undergoing Arthroplasty

Arthroplasty Clinical Trial

Official title:
Risk Factors for Acute Kidney Injury in Patients Undergoing Total Joint Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06296108
Other study ID # I05-310-22
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2022
Est. completion date December 31, 2022

Study information
Verified date March 2024
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The authors aimed to determine the risk factors associated with postoperative acute kidney injury in patients undergoing total joint arthroplasty.

Description:

Aim: The primary aim of the current study is to determine the risk factors associated with postoperative acute kidney injury in patients undergoing total joint arthroplasty. Considering that this patient group is mostly composed of advanced age and comorbid patients, the secondary aim of the study is to identify risky patients with predictable risk factors and to chart a way to make preoperative optimizations of the patients before developing postoperative complications. Materials and Methods: Patients who underwent joint arthroplasty between 2015 and 2020 in Ankara University Faculty of Medicine, Department of Orthopedics and Traumatology were included. Within the scope of the study, patients' gender, age, weight, height, body mass index values, smoking, American Society of Anesthesiologist (ASA) score, Charlson-Comorbidity Index score (CCI), type of operation, duration of surgery, presence of intraoperative hypotension, anesthesia method , diabetes, hypertension, coronary artery disease, presence of congestive heart failure, presence of preoperative anemia, preoperative uric acid and albumin level, use of nephrotoxic agents in the perioperative period, basal creatinine and glomerular filtration rate (GFR) values, platelet suspension in the perioperative period, erythrocyte suspension, Amounts of fresh frozen plasma transfusions, postoperative creatinine at 24 hours - 48 hours - discharge, GFR values and Kidney Disesae Improving Global Outcomes (KDIGO) scores, length of hospital stay and length of stay in the intensive care unit were evaluated.

Recruitment information / eligibility
Status Completed
Enrollment 911
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients aged above 18 years old undergoing arthroplasty surgery Exclusion Criteria: - Known acute renal failure or chronic renal failure - Patients aged below 18 years old - Patients refusing to participate to the study

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• acute kidney injury
The incidence of acute kidney injury was determined in patients included to the study

Locations
Country Name City State
Turkey Ankara University Medical School Anesthesiology and ICU Department Ankara

Sponsors (1)
Lead Sponsor Collaborator
Ankara University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Acute kidney injury in patients undergoing arthroplasty surgery To determine the incidence of acute kidney injury in patients undergoing arthroplasty surgery Retrospective between 2015-2020
Secondary Risk factors causing acute kidney injury in patients undergoing arthroplasty surgery To determine the risk factors causing acute kidney injury in patients undergoing arthroplasty surgery Retrospective between 2015-2020
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