Monitoring of Dialysis Vascular Accesses During Angioplasty Under Echodoppler
NCT ID: NCT05545267
Last Updated: 2022-09-19
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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UNKNOWN
144 participants
OBSERVATIONAL
2021-09-17
2022-10-31
Brief Summary
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The complication rates of ultrasound angioplasty remain poorly known because only a few series have been published. In addition, the evolution of the echo-Doppler parameters of the AVF is unknown during angioplasty and it is difficult to know which are the most reliable to distinguish during the procedure a "good angioplasty gesture" from an incomplete angioplasty to be continued. The proposed study would provide initial insight into the question posed.
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Detailed Description
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In order to establish the evolution of the echographic parameters over time, the echographic data will also be collected from each follow-up report corresponding to each procedure until the end of the follow-up. These reports correspond to the normal post-intervention control ultrasounds at 1 month, 3 months and the annual visits. If intermediate ultrasounds are available, their reports will also be used.
In the case of a patient having an emergency angioplasty, the data of the control ultrasound triggering the intervention will be used as pre-intervention data.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Interventions
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Angioplasties
Transluminal angioplastie
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patient undergoing whose fistula is treated by angioplasty under echo-doplerat the Vichy Hospital Center between 01/01/2015 and 31/12/2019
Exclusion Criteria
* Patients with an AVF with a flow rate \< 100 mL/min.
* Patients with acute or chronic, segmental or total occlusion of an AVF segment
* Patients with acute or chronic, segmental or total thrombosis of an AVF segment
* Patients whose main obstacle is located on the arterial side.
* Intervention that required the use of X-rays.
18 Years
ALL
No
Sponsors
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Centre Hospitalier de Vichy
OTHER
Responsible Party
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Principal Investigators
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Fabrice ABBADIE
Role: STUDY_DIRECTOR
Centre hopsitalier de Vichy
Locations
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Centre Hospitalier de Vichy (CHV)
Vichy, , France
Countries
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Other Identifiers
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SAVE1 - CHV 2018-2
Identifier Type: -
Identifier Source: org_study_id
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