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NCT02322567 Clinical Trial

Left Ventricular Diastolic Dysfunction in Kidney Recipients

Kidney Transplantation Clinical Trial

Official title:
Influence of Left Ventricular Diastolic Dysfunction on Graft Function and Postoperative Complication in Patients Undergoing Elective Kidney Transplantation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02322567
Other study ID # 4-2014-0808
Secondary ID
Status Completed
Phase N/A
First received December 9, 2014
Last updated February 24, 2016
Start date January 2012
Est. completion date October 2015

Study information
Verified date February 2016
Source Severance Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to examine the relationship between pre-operative LV diastolic function and post-operative complications and kidney function in living-donor kidney transplantation patients.

Recruitment information / eligibility
Status Completed
Enrollment 242
Est. completion date October 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender Both
Age group 19 Years to 70 Years
Eligibility Inclusion Criteria:

- Elective kidney transplantation patients

Exclusion Criteria:

- No data of preoperative echocardiography

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Other:
• medical records
review of medical records

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine and Anesthesia and Pain Research Institute, Yonsei University College of Medicine Seoul

Sponsors (1)
Lead Sponsor Collaborator
Severance Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Other Postoperative graft function (graft failure, acute rejection, graft loss, serum creatinine) graft failure, acute rejection, graft loss, serum creatinine 30 days Yes
Primary Patients with postoperative cardiovascular complications acute myocardial infarction, ventricular fibrillation/tachycardia, cardiogenic shock, newly-onset atrial fibrillation, clinical pulmonary edema requiring endotracheal intubation or dialysis 30 days Yes
Secondary Patients with postoperative pulmonary edema pulmonary edema by radiological evidence 30 days Yes
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