Identifying Risk Factors (RF) for Early Haemodialysis Arteriovenous Fistula Failure (eAVFF)
NCT ID: NCT05552482
Last Updated: 2023-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
105 participants
OBSERVATIONAL
2021-01-05
2022-12-21
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Patients with ESRD with early AVF failure
Patients with ESRD who underwent AVF access creation surgery with early AVF failure
Identification of predictive factors
Evaluation of the following variables : age, sex, body mass index, Diabetes mellitus, vascular disease, hematologic disease, venous thromboembolic disease, antiplatelet or anticoagulant treatments, haemodialysis Catheter Insertion, number of comorbid conditions, Venous diameter, Arterial diameter, AVF type, AVF limb, Anasthesia group
patients with ESRD without early AVF failure
Patients with ESRD who underwent AVF access creation surgery without early AVF failure
Identification of predictive factors
Evaluation of the following variables : age, sex, body mass index, Diabetes mellitus, vascular disease, hematologic disease, venous thromboembolic disease, antiplatelet or anticoagulant treatments, haemodialysis Catheter Insertion, number of comorbid conditions, Venous diameter, Arterial diameter, AVF type, AVF limb, Anasthesia group
Interventions
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Identification of predictive factors
Evaluation of the following variables : age, sex, body mass index, Diabetes mellitus, vascular disease, hematologic disease, venous thromboembolic disease, antiplatelet or anticoagulant treatments, haemodialysis Catheter Insertion, number of comorbid conditions, Venous diameter, Arterial diameter, AVF type, AVF limb, Anasthesia group
Eligibility Criteria
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Inclusion Criteria
* Patients who had undergone distal (radioradial and radiocephalic) or proximal arteriovenous fistula (AVF) access creation surgery between 2016 and 2021 at the CHR Metz-Thionville.
* Patients who underwent preoperative and postoperative Doppler ultrasound (DUS) ≤ 4 months after surgery.
* Patients with central venous catheter (CVC) at surgery
Exclusion Criteria
* Patients with a radiobasilic AVF or arteriovenous graft
18 Years
ALL
No
Sponsors
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Centre Hospitalier Régional Metz-Thionville
OTHER
Responsible Party
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Principal Investigators
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Zead TUBAIL, MD
Role: PRINCIPAL_INVESTIGATOR
CHR Metz Thionville Hopital de Mercy
Locations
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CHR Metz-Thionville/Hopital de Mercy
Metz, , France
Countries
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Other Identifiers
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2022-06Obs-CHRMT
Identifier Type: -
Identifier Source: org_study_id
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