Skip to content

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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05894317
Acronym
VACTANE
Enrollment
60
Registered
2023-06-08
Start date
2020-06-01
Completion date
2025-02-14
Last updated
2025-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Apheresis Related Complication, Vascular Access Complication

Keywords

Apheresis, DFPP, ANCA associated vasculitis, Goodpasture syndrome, Arterio veinous fistula, Arterio veinous graft

Brief 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.

Interventions

None listed

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* patients in nephrology receiveing apheresis treatment by filtration or double filtration

Exclusion criteria

* apheresis treatment for other indications * centrifugation apheresis treatment

Design outcomes

Primary

MeasureTime frameDescription
Vascular access Complication (catheter or AVF/AVG thrombosis/infection) rate in therapeutic apheresis among nephrological diseasesjune 2020 june 2022Percent of patient with Vascular access Complication

Secondary

MeasureTime frameDescription
Description of population enrolledjune 2020 june 2022Description of population treated by therapeutic apheresis in Northeast France
Comparison of complications rate with literature datasjune 2020 june 2022

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026