Complications Related to Vascular Access Devices in Home Parenteral Nutrition Patients
NCT ID: NCT05948514
Last Updated: 2023-07-17
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
300 participants
OBSERVATIONAL
2017-07-01
2020-12-30
Brief Summary
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The aim of this prospective cohort study is to compare the incidence rate of catheter related complications among 3 types of central vascular access: peripherally inserted central catheters; tunneled catheters and port-a-cath devices, in adults patients on HPN; describe the risk factors, and identify a potential link between venous thromboembolism and infection.
More than 300 patients will be consecutively enrolled and followed up from the time of catheter insertion until its removal. Venous complication (identify by an ultrasound examination if deep vein thrombosis is suspected), infection related to catheter and mechanical complications will be analyzed. The incidence of complications will be expressed per 1000 catheters-day and or as a percentage of total catheter.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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adult patients followed up in the nutrition and access device was inserted for parenteral nutrition
no intervention, observational study patients are enrolled, and followed up until a catheter related complication occurs
The complications related to central venous access device
The complications related to central venous access device were collected when occurs : from time of catheter insertion, until first complication, or removal for another type of catheter, or until death.
Interventions
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The complications related to central venous access device
The complications related to central venous access device were collected when occurs : from time of catheter insertion, until first complication, or removal for another type of catheter, or until death.
Eligibility Criteria
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Inclusion Criteria
* having a catheter insertion during the study periode
* at the unit of vascular access of Lyon Sud Hospital
* for parenteral nutrition
* from July 1st, 2017 to June 30, 2020
Exclusion Criteria
* for other treatment (chemotherapy, antibiotic)
18 Years
ALL
No
Sponsors
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Hospices Civils de Lyon
OTHER
Responsible Party
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Locations
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Centre Hospitalier Lyon Sud-Hospices Civils de Lyon
Pierre-Bénite, , France
Countries
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Other Identifiers
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69HCL22_1128
Identifier Type: -
Identifier Source: org_study_id
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