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
50 participants
OBSERVATIONAL
2008-11-30
2009-03-31
Brief Summary
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Inclusion criteria and study design are detailed below.
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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1
Chronic hemodialysis patients, native arterio-venous fistula
Buttonhole cannulation with semi-blunt needles
Use of semi-blunt needles, compared to blunt needles, at every dialysis session
2
Chronic hemodialysis patients, native arterio-venous fistula
Buttonhole cannulation with semi-blunt needles
Use of semi-blunt needles, compared to blunt needles, at every dialysis session
Interventions
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Buttonhole cannulation with semi-blunt needles
Use of semi-blunt needles, compared to blunt needles, at every dialysis session
Eligibility Criteria
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Inclusion Criteria
* Aged 18 years or more
* Dialyzed by a native arterio-venous fistula
* Cannuled by buttonhole method with blunt needles
Exclusion Criteria
* Puncture with 14G needles
* Puncture with a sole needle
* Arterio-venous grafts
* Patients transferred from another centre
18 Years
ALL
No
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Cliniques Universitaires Saint-Luc, Université Catholique de Louvain
Principal Investigators
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Laura Labriola, M.D.
Role: PRINCIPAL_INVESTIGATOR
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Locations
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Cliniques Universitaires Saint Luc
Brussels, , Belgium
Countries
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Other Identifiers
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Semi-blunt needles
Identifier Type: -
Identifier Source: secondary_id
Needles
Identifier Type: -
Identifier Source: org_study_id