drug-coated balloon catheter (Orchid, Acotec)
DeviceAfter predilation, using drug-coated balloon catheter to cover the whole treated segment
NCT Number: NCT03366727
This trial is aimed to evaluate the safety and efficacy of DCB in treating AVF stenosis in chinese population.
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Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Chinese PLA General Hospital, Beijing, Beijing Municipality, China
For years, first-line treatment of AVFs stenoses has been percutaneous transluminal angioplasty. However, restenosis and reintervention rates remain incredibly high and occur, according to recent studies, in up to 60% and 70% of patients at 6 and 12 months, respectively. Drug-coated balloons delivering paclitaxel at the angioplasty site have proved their superiority in the treatment of coronary and peripheral arterial stenoses. Paclitaxel reduces neointimal hyperplasia and drug-coated balloons,therefore, it represents an attractive option for AVF stenoses.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
After predilation, using drug-coated balloon catheter to cover the whole treated segment
After predilation, using plain balloon catheter to cover the whole treated segment
Time frame: 6 months
Primary Patency is defined as the freedom of reintervention for the target lesion,including: 1)clinical driven target lesion reintervention;2)thrombus formation in target lesion; 3) surgical removal of target lesion;4) AVF was abandoned because of the target lesion could not be retreated
Time frame: 12 months
Primary Patency is defined as the freedom of reintervention for the target lesion,including: 1)clinical driven target lesion reintervention;2)thrombus formation in target lesion; 3) surgical removal of target lesion;4) AVF was abandoned because of the target lesion could not be retreated
Time frame: 12 months
number of reinterventions in 12 months
Time frame: during the procedure
Successful delivery to the target lesion, deployment, and retrieval at index procedure
Time frame: 5 days
The resumption of dialysis for at least one session after the index procedure
Time frame: 2 weeks
residual stenosis≤30% and absence of SAE during perioperative period
Acotec Scientific Co., Ltd
Industry
Drug-eluting Balloon for Arteriovenous Fistula in China
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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