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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04979754
Other study ID # SAR Sud study one
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2020
Est. completion date September 30, 2021

Study information

Verified date December 2021
Source University Hospital, Bordeaux
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this retrospective study, the authors assess long term renal outcome in renal transplant recipients after cardiac surgery with cardiopulmonary bypass, and research factors associated with poor long term renal outcome.


Description:

Post-operative mortality after cardiac surgery is increased in renal transplant recipients, compared with general population of cardiac surgery, or with kidney transplant recipients not undergoing cardiac surgery. If the survival of this specific population is now well studied, the long-term renal outcome is much less studied. Previous studies show a trend for increased risk of allograft dysfunction and need for permanent dialysis. This study proposes to compare long term renal outcome between renal transplant recipients and non-renal transplant recipients.


Recruitment information / eligibility

Status Completed
Enrollment 93
Est. completion date September 30, 2021
Est. primary completion date August 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria for Renal Transplant Recipients group: - Previous renal transplantation - Who underwent cardiac surgery with CPB Inclusion Criteria for Non Renal Transplant Récipients group: - No previous renal transplantation - Who underwent cardiac surgery with CPB - Apparied with Renal Transplant récipients with the 5 following criteria : age, sex, previous diagnosis of diabete, type of cardiac surgery (isolated coronary artery bypass graft, valvular surgery, aorta surgery, combined surgery), best glomerular filtration rate with CKD-EPI formula at +/- 15 ml/min, in the 3 pre-operative months Exclusion Criteria: - Patients requiring mechanical circulatory support (Extracorporeal Membrane Oxygenation) - Pre-operative permanent dialysis - Aorta dissection extended to renal arteries - Non-elective surgery for infective endocarditis - Previous hepatic, pancreatic or cardiac transplantation - Death in the 30 first days after cardiac surgery - Patient not meeting the inclusion criteria

Study Design


Intervention

Other:
standard of care
retrospective study : standard of care

Locations

Country Name City State
France Bordeaux University Hospital Pessac

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Long-term renal outcome Proportion of patients meeting a composite criterion : death or permanent dialysis or doubling the baseline serum creatinine value 12 months after surgery
Secondary Glomerular Filtration Rate (GFR) Glomerular Filtration Rate (GFR) calculated with CKD-EPI formula 30 days after surgery
Secondary Glomerular Filtration Rate (GFR) Glomerular Filtration Rate (GFR) calculated with CKD-EPI formula 12 months after surgery
Secondary Vital status Mortality after surgery 12 months after surgery
Secondary Major Adverse Kidney Events Major Adverse Kidney Events defined by new receipt of Renal replacement therapy (RRT), or Acute Kidney Injury (AKI) episodes with persistent renal dysfunction and final serum creatinine value before hospital discharge = 200 % of the baseline serum creatinine Up to 12 months after surgery
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