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Completed

NCT Number: NCT03366727

AcoArt III / Arterio-venous Fistula in China

This trial is aimed to evaluate the safety and efficacy of DCB in treating AVF stenosis in chinese population.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chinese PLA General Hospital, Beijing, Beijing Municipality, China

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age during 18-85 years old
  • Arteriovenous fistula is matured and has undergone one or more hemodialysis sessions
  • Venous stenosis of the AV fistula
  • target lesion has stenosis ≥50% evidenced by angiography. and have at least one symptom of these:1,the venous pressure increased significantly during dialysis. 2,abnormal physical examination. 3,Decrease in blood flow
  • the length of target lesion ≤100mm
  • Patient able to give informed consent
  • residual stenosis ≤30% after predilation

Exclusion criteria

  • Women who are breastfeeding, pregnant or are intending to become pregnant
  • AVF located at lower limbs
  • two or more than two stenosis at the target vessel.
  • Obstruction of central venous return
  • ISR
  • AVF with acute thrombosis requiring lysis or thrombectomy in 30 days
  • vascular access has surgery in 30 days or intending to undergo a surgery
  • known hypersensitivity to aspirin, heparin, clopidogrel,paclitaxel, contrast medium, etc.
  • Patients undergoing immunotherapy or suspected / confirmed vasculitis
  • Patients with history of blood coagulation dysfunction and history of thrombocytopenic purpura
  • Vascular access infection or systemic active infection
  • patients's life expectancy is less than 12 months
  • Renal transplantation has been planned or converted to peritoneal dialysis
  • Other medical conditions that lead to researchers who believe that patients may not be able to follow the trial program
  • involved in other drugs, biology, medical device research, or has been involved in other similar products clinical Test

Treatment and study plan

drug-coated balloon catheter (Orchid, Acotec)

Device

After predilation, using drug-coated balloon catheter to cover the whole treated segment

plain balloon catheter (Admiral, medtronic)

Device

After predilation, using plain balloon catheter to cover the whole treated segment

Primary outcomes

  1. primary patency of target lesion in 6 months

    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

Secondary outcomes

  1. primary patency of target lesion in 12 months

    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

  2. number of reinterventions

    Time frame: 12 months

    number of reinterventions in 12 months

  3. device success

    Time frame: during the procedure

    Successful delivery to the target lesion, deployment, and retrieval at index procedure

  4. clinical success

    Time frame: 5 days

    The resumption of dialysis for at least one session after the index procedure

  5. Procedural Success

    Time frame: 2 weeks

    residual stenosis≤30% and absence of SAE during perioperative period

Sponsors and collaborators

Lead sponsor

Acotec Scientific Co., Ltd

Industry

Registry information

Official study title

Drug-eluting Balloon for Arteriovenous Fistula in China

Important dates

Study start
2018
Primary completion
2021
Study completion
2022
First posted
Dec 8, 2017
Registry last updated
Jul 27, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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