Dialysis Access Malfunction
Conditions
Keywords
Paclitaxel coated balloon, Cutting balloon, Recurrent stenosis
Brief summary
To determine if cutting balloon angioplasty combined with DEB angioplasty provides a higher primary patency after treatment of recurrent stenoses compared with cutting balloon angioplasty or angioplasty using DEB alone in the venous outflow AVFs. For cutting balloon angioplasty in venous stenosis, the primary patency after 12 months is 55-60% (9,16) and in recurrent stenoses up to 48%(10). We hypothesise that DEB angioplasty after cutting balloon angioplasty leads to improved primary patency at 12 months.
Interventions
DEVICECutting balloon followed by paclitaxel coated balloon
Cutting balloon followed by paclitaxel coated balloon
Sponsors
Boston Scientific Corporation
Singapore General Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Recurrent stenoses (within 1 year after angioplasty) in the venous outflow of AVFs for dialysis access (\> 0.5cm from AV anastomosis up to cephalic arch) * Successful guidewire crossing of target lesion * ≥ 21 years old * Informed and valid consent given. * Patient willing and able to return for follow up .
Exclusion criteria
1. Thrombosed AVFs or occlusions in the access circuit 2. Significant cephalic arch (central perpendicular portion of the cephalic vein) or central vein stenoses. 3. \> 3 stenosed segments (lesions are considered separate if they are separated by at least 2 cm normal vessel.) 4. Only potential target lesion located in cephalic arch, central veins or anastomotic lesions. 5. Only de novo stenoses identifiable as target lesion. 6. Target lesion resistant to cutting balloon angioplasty (\>30% residual stenosis with incomplete effacement of the lesion during cutting balloon angioplasty) 7. Target lesion not treatable with the available sizes of cutting balloon (4-7mm) and drug eluting balloon (up to 8mm) so native reference vessel \<3 mm or need for DEB balloon \>8mm. 8. Lesion in excess of 8 cm 9. Unable to take dual antiplatelet therapy for 1 month and/or aspirin for 6 months 10. Coagulopathy (PT or PTT \>1.5 times the median of normal range) or thrombocytopenia (platelet count \<50,000 /μL) that cannot be managed adequately with periprocedural transfusion. 11. Patient on Warfarin. 12. Known allergy to iodinated contrast that cannot be managed adequately with pre-procedure medication. 13. Allergy / contraindication to dual anti-platelet therapy (aspirin and clopidogrel or ticlopidine) or paclitaxel. 14. Acute infection over proposed puncture site. 15. Women who are breastfeeding, pregnant or planning on becoming pregnant during study. 16. Participant with medical conditions, which in the opinion of the investigator may cause non-compliance with protocol. 17. Currently participating in an investigational drug, biologic or device trial that may have an impact on the dialysis access or previous enrolment in this study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Target lesion primary patency | 1 year | Target lesion primary patency |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Circuit primary patency | 1 year | Circuit primary patency |
| Target lesion primary assisted patency | 1 year | — |
Countries
Singapore
Outcome results
None listed