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Trials / Completed

CompletedNCT05894317

Vascular Access Complications for Therapeutic Apheresis in Nephrology

Vascular Access Complications for Therapeutic Apheresis in Nephrology : a Retrospective Observational Study in North-East France.

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
Central Hospital, Nancy, France · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to describe vascular access complications which are used for therapeutic apheresis in Nephrology.

Detailed description

The aim of this study is to describe vascular access complications which are used for therapeutic apheresis in Nephrology. Complications may include arterio-veinous fistula or graft (AVF or AVG) thrombosis with or without known stenosis; AVF or AVG or central veinous catheter (CVC) infections and CVC dysfunctions. The investigators may enroll all patients receveing therapeutic apheresis for nephrologic indications in North East France. Nephrologics indications include : * acute or active antibody mediated rejection (ABMR), * Goodpasture disease, * ANCA vasculitis, * thrombotic microangiopathy (TMA), * Focal segmental glomerulosclerosis (FSGS), * HLA or ABO desensitization for kidney transplantation. Data inclusion period is from June 2020 to June 2022. The aim of the study is to describe the proportion and type of complication in the population of patient receving therapeutic apheresis for nephrologic disease in the North East France. Te investigators will study the risk factors that are associated with this complications. The second aim of the study is to describe the population of patient receving therapeutic apheresis in our unit and in our region.

Conditions

Timeline

Start date
2020-06-01
Primary completion
2022-06-30
Completion
2025-02-14
First posted
2023-06-08
Last updated
2025-02-24

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05894317. Inclusion in this directory is not an endorsement.