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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06280898
Other study ID # KC22RISI0395
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date March 14, 2022

Study information

Verified date February 2024
Source Seoul St. Mary's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Divided into two groups based on acute kidney injury: non-acute kidney injury group vs. non-acute kidney injury group. Acute kidney injury group, Acute Kidney Injury Network (AKIN), Risk, Injury, Failure, Loss of kidney function, and End-stage kidney disease (RIFLE), or Kidney Disease: Improving Global Outcomes (KDIGO) I would like to divide it according to the definition. After testing the normal distribution of patients, donors, grafts, types of immunosuppressants, surgery/anesthesia factors, and blood test findings between the two groups through the Shapiro-Wilk test, continuous data was tested using the student t-test or Mann-Whitney U test. Sizes are compared using , and categorical data is compared with proportions using the χ2 test or Fisher's exact test. Analysis of factors related to acute kidney injury will be performed through univariate and multivariate logistic regression analysis.


Recruitment information / eligibility

Status Completed
Enrollment 539
Est. completion date March 14, 2022
Est. primary completion date March 14, 2022
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria: - Adult patients aged 19 years or older who underwent kidney transplant surgery in the operating room Exclusion Criteria: - Pediatric patients under 19 years of age - Patients with multiple organ transplants, including kidney transplants - Patients undergoing re-kidney transplant surgery - Patient examination findings missing from electronic medical record

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Remote ischemic conditioning
Remote ischemic condition

Locations

Country Name City State
Korea, Republic of Seoul St. Mary's hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul St. Mary's Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Troponin I Troponin I difference in two groups up to 24 hour postoperatively
Secondary Troponin T Troponin T difference in two groups up to 24 hour postoperatively
Secondary QTc interval OTc interval difference in two groups up to 24 hour postoperatively
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