External Ionizing Radiation to Prevent Restenosis on Haemodialysis Vascular Access
NCT ID: NCT00379366
Last Updated: 2015-03-18
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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TERMINATED
PHASE2/PHASE3
5 participants
INTERVENTIONAL
2006-12-31
2009-01-31
Brief Summary
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Detailed Description
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Objective: the main objective is to assess external ionizing radiation for restenosis prevention on prosthetic haemodialysis vascular accesses after angioplasty. A secondary objective is to assess the treatment safety.
Methods: Single blind randomized clinical trial on two parallel groups of 53 patients each. Patients with chronic renal failure treated by dialysis will be included after a successful angioplasty on a stenosis of the vein adjacent to their prosthetic haemodialysis vascular access. One group will be treated by a single dose of ionizing radiations (14 Gy) at day 1 after angioplasty. The control group will not receive any preventive treatment. The primary outcome is the one-year vascular access patency failure. Secondary outcomes are the one-year delay of occurrence of a restenosis and the treatment safety. Outcomes will be assessed by a clinical and ultrasonographic (at 1, 3, 6 and 12 months, or at other time points in case of stenosis suspicion) follow-up.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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1
14 Gy ionizing radiations
External ionizing radiations
14 Gy in one time
2
No interventions assigned to this group
Interventions
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External ionizing radiations
14 Gy in one time
Eligibility Criteria
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Inclusion Criteria
* successful angioplasty (residual stenosis \< 30%) on a significant stenosis (maximal systolic speed 3 times \> from basal maximal systolic speed, stenosis \> 70% on angiography) on the venous-prosthesis anastomosis or on the venous segment 5 cm after the anastomosis of a prosthetic haemodialysis vascular access (at least 1 month old)
* social security affiliation
* signed informed consent
Exclusion Criteria
* angioplasty with stenting
18 Years
ALL
No
Sponsors
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Ministry of Health, France
OTHER_GOV
University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Jean-Philippe MAIRE, Pr
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Bordeaux, France
Paul Perez, Dr
Role: STUDY_CHAIR
University Hospital, Bordeaux, France
Locations
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Clinc Delay
Bayonne, , France
Côte Basque Hospital
Bayonne, , France
Clinic Saint Augustin
Bordeaux, , France
Service de Chirurgie Vasculaire, Hôpital Pellegrin-tripode, CHU de Bordeaux
Bordeaux, , France
Clinic Francheville
Périgueux, , France
Countries
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Other Identifiers
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2005-011
Identifier Type: -
Identifier Source: secondary_id
9443-05
Identifier Type: -
Identifier Source: org_study_id
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